Canonical Allele Identifier: CA1923816317
Gene: NRG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.82886273_82886281delinsTATGCCCTC , CM000672.2:g.82886273_82886281delinsTATGCCCTC GRCh38
NC_000010.10:g.84646029_84646037delinsTATGCCCTC , CM000672.1:g.84646029_84646037delinsTATGCCCTC GRCh37
NC_000010.9:g.84636009_84636017delinsTATGCCCTC NCBI36
NG_013373.1:g.1015960_1015968delinsTATGCCCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000372141.7:c.1054+20836_1054+20844delinsTATGCCCTC MANE Select ENSP00000361214.2:n.1054+20836_1054+20844...
ENST00000372141.6:c.1054+20836_1054+20844delinsTATGCCCTC ENSP00000361214.2:n.1054+20836_1054+20844...
ENST00000372142.6:c.391+20836_391+20844delinsTATGCCCTC ENSP00000361215.2:n.391+20836_391+20844de...
ENST00000404547.5:c.1054+20836_1054+20844delinsTATGCCCTC ENSP00000384796.1:n.1054+20836_1054+20844...
ENST00000404576.6:c.466+20836_466+20844delinsTATGCCCTC ENSP00000385804.2:n.466+20836_466+20844de...
ENST00000537893.1:c.4+20836_4+20844delinsTATGCCCTC ENSP00000440377.1:n.4+20836_4+20844delins...
ENST00000545131.5:c.4+20836_4+20844delinsTATGCCCTC ENSP00000441201.1:n.4+20836_4+20844delins...
ENST00000555784.5:c.454+20836_454+20844delinsTATGCCCTC ENSP00000451858.1:n.454+20836_454+20844de...
ENST00000556918.5:c.544+20836_544+20844delinsTATGCCCTC ENSP00000451376.1:n.544+20836_544+20844de...
ENST00000602794.5:c.*690+20836_*690+20844delinsTATGCCCTC ENSP00000473669.1:n.*690+20836_*690+20844...
NM_001010848.3:c.1054+20836_1054+20844delinsTATGCCCTC NP_001010848.2:n.1054+20836_1054+20844del...
NM_001165972.1:c.1051+20836_1051+20844delinsTATGCCCTC NP_001159444.1:n.1051+20836_1051+20844del...
NM_001165973.1:c.391+20836_391+20844delinsTATGCCCTC NP_001159445.1:n.391+20836_391+20844delin...
XM_005269444.3:c.1054+20836_1054+20844delinsTATGCCCTC XP_005269501.1:n.1054+20836_1054+20844del...
XM_011539172.1:c.1054+20836_1054+20844delinsTATGCCCTC XP_011537474.1:n.1054+20836_1054+20844del...
XM_011539173.1:c.1051+20836_1051+20844delinsTATGCCCTC XP_011537475.1:n.1051+20836_1051+20844del...
XM_011539174.1:c.1028-65196_1028-65188delinsTATGCCCTC XP_011537476.1:n.1028-65196_1028-65188del...
XM_011539175.1:c.1054+20836_1054+20844delinsTATGCCCTC XP_011537477.1:n.1054+20836_1054+20844del...
XM_011539176.1:c.274+20836_274+20844delinsTATGCCCTC XP_011537478.1:n.274+20836_274+20844delin...
XM_011539177.1:c.274+20836_274+20844delinsTATGCCCTC XP_011537479.1:n.274+20836_274+20844delin...
XM_011539179.1:c.4+20836_4+20844delinsTATGCCCTC XP_011537481.1:n.4+20836_4+20844delinsTAT...
XM_005269444.5:c.1054+20836_1054+20844delinsTATGCCCTC XP_005269501.1:n.1054+20836_1054+20844del...
XM_011539172.3:c.1054+20836_1054+20844delinsTATGCCCTC XP_011537474.1:n.1054+20836_1054+20844del...
XM_011539173.3:c.1051+20836_1051+20844delinsTATGCCCTC XP_011537475.1:n.1051+20836_1051+20844del...
XM_011539175.3:c.1054+20836_1054+20844delinsTATGCCCTC XP_011537477.1:n.1054+20836_1054+20844del...
XM_017015573.2:c.1132+20836_1132+20844delinsTATGCCCTC XP_016871062.1:n.1132+20836_1132+20844del...
XM_017015574.2:c.1132+20836_1132+20844delinsTATGCCCTC XP_016871063.1:n.1132+20836_1132+20844del...
XM_017015575.2:c.1129+20836_1129+20844delinsTATGCCCTC XP_016871064.1:n.1129+20836_1129+20844del...
XM_017015576.2:c.1129+20836_1129+20844delinsTATGCCCTC XP_016871065.1:n.1129+20836_1129+20844del...
XM_017015577.2:c.1132+20836_1132+20844delinsTATGCCCTC XP_016871066.1:n.1132+20836_1132+20844del...
XM_017015578.2:c.1132+20836_1132+20844delinsTATGCCCTC XP_016871067.1:n.1132+20836_1132+20844del...
XM_017015579.2:c.1129+20836_1129+20844delinsTATGCCCTC XP_016871068.1:n.1129+20836_1129+20844del...
XM_017015580.2:c.1129+20836_1129+20844delinsTATGCCCTC XP_016871069.1:n.1129+20836_1129+20844del...
XM_017015581.2:c.1051+20836_1051+20844delinsTATGCCCTC XP_016871070.1:n.1051+20836_1051+20844del...
XM_017015582.1:c.274+20836_274+20844delinsTATGCCCTC XP_016871071.1:n.274+20836_274+20844delin...
XM_017015583.1:c.274+20836_274+20844delinsTATGCCCTC XP_016871072.1:n.274+20836_274+20844delin...
XM_024447781.1:c.4+20836_4+20844delinsTATGCCCTC XP_024303549.1:n.4+20836_4+20844delinsTAT...
XR_001747009.2:n.1283+20836_1283+20844delinsTATGCCCTC
NM_001010848.4:c.1054+20836_1054+20844delinsTATGCCCTC MANE Select NP_001010848.2:n.1054+20836_1054+20844del...
NM_001370081.1:c.1051+20836_1051+20844delinsTATGCCCTC NP_001357010.1:n.1051+20836_1051+20844del...
NM_001370082.1:c.487+20836_487+20844delinsTATGCCCTC NP_001357011.1:n.487+20836_487+20844delin...
NM_001370084.1:c.1054+20836_1054+20844delinsTATGCCCTC NP_001357013.1:n.1054+20836_1054+20844del...
NR_163251.1:n.1402+20836_1402+20844delinsTATGCCCTC
NR_163252.1:n.637+20836_637+20844delinsTATGCCCTC
NR_163253.1:n.1129+20836_1129+20844delinsTATGCCCTC
NM_001165973.2:c.391+20836_391+20844delinsTATGCCCTC NP_001159445.1:n.391+20836_391+20844delin...