Canonical Allele Identifier: CA1923424000
Gene: NRG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.82059367_82059369delinsGAT , CM000672.2:g.82059367_82059369delinsGAT GRCh38
NC_000010.10:g.83819123_83819125delinsGAT , CM000672.1:g.83819123_83819125delinsGAT GRCh37
NC_000010.9:g.83809103_83809105delinsGAT NCBI36
NG_013373.1:g.189054_189056delinsGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000372141.7:c.823+183204_823+183206delinsGAT MANE Select ENSP00000361214.2:n.823+183204_823+183206...
ENST00000372141.6:c.823+183204_823+183206delinsGAT ENSP00000361214.2:n.823+183204_823+183206...
ENST00000372142.6:c.61-107360_61-107358delinsGAT ENSP00000361215.2:n.61-107360_61-107358de...
ENST00000404547.5:c.823+183204_823+183206delinsGAT ENSP00000384796.1:n.823+183204_823+183206...
ENST00000404576.6:c.136-107360_136-107358delinsGAT ENSP00000385804.2:n.136-107360_136-107358...
ENST00000555784.5:c.135+181272_135+181274delinsGAT ENSP00000451858.1:n.135+181272_135+181274...
ENST00000556918.5:c.136-107360_136-107358delinsGAT ENSP00000451376.1:n.136-107360_136-107358...
ENST00000602794.5:c.*371+169702_*371+169704delinsGAT ENSP00000473669.1:n.*371+169702_*371+1697...
NM_001010848.3:c.823+183204_823+183206delinsGAT NP_001010848.2:n.823+183204_823+183206del...
NM_001165972.1:c.823+183204_823+183206delinsGAT NP_001159444.1:n.823+183204_823+183206del...
NM_001165973.1:c.61-107360_61-107358delinsGAT NP_001159445.1:n.61-107360_61-107358delin...
XM_005269444.3:c.823+183204_823+183206delinsGAT XP_005269501.1:n.823+183204_823+183206del...
XM_011539172.1:c.823+183204_823+183206delinsGAT XP_011537474.1:n.823+183204_823+183206del...
XM_011539173.1:c.823+183204_823+183206delinsGAT XP_011537475.1:n.823+183204_823+183206del...
XM_011539174.1:c.823+183204_823+183206delinsGAT XP_011537476.1:n.823+183204_823+183206del...
XM_011539175.1:c.823+183204_823+183206delinsGAT XP_011537477.1:n.823+183204_823+183206del...
XM_005269444.5:c.823+183204_823+183206delinsGAT XP_005269501.1:n.823+183204_823+183206del...
XM_011539172.3:c.823+183204_823+183206delinsGAT XP_011537474.1:n.823+183204_823+183206del...
XM_011539173.3:c.823+183204_823+183206delinsGAT XP_011537475.1:n.823+183204_823+183206del...
XM_011539175.3:c.823+183204_823+183206delinsGAT XP_011537477.1:n.823+183204_823+183206del...
XM_017015573.2:c.824-173375_824-173373delinsGAT XP_016871062.1:n.824-173375_824-173373del...
XM_017015574.2:c.824-173375_824-173373delinsGAT XP_016871063.1:n.824-173375_824-173373del...
XM_017015575.2:c.824-173375_824-173373delinsGAT XP_016871064.1:n.824-173375_824-173373del...
XM_017015576.2:c.824-173375_824-173373delinsGAT XP_016871065.1:n.824-173375_824-173373del...
XM_017015577.2:c.824-173375_824-173373delinsGAT XP_016871066.1:n.824-173375_824-173373del...
XM_017015578.2:c.824-173375_824-173373delinsGAT XP_016871067.1:n.824-173375_824-173373del...
XM_017015579.2:c.824-173375_824-173373delinsGAT XP_016871068.1:n.824-173375_824-173373del...
XM_017015580.2:c.824-173375_824-173373delinsGAT XP_016871069.1:n.824-173375_824-173373del...
XM_017015581.2:c.823+183204_823+183206delinsGAT XP_016871070.1:n.823+183204_823+183206del...
XM_017015584.2:c.824-173375_824-173373delinsGAT XP_016871073.1:n.824-173375_824-173373del...
XR_001747009.2:n.975-173375_975-173373delinsGAT
NM_001010848.4:c.823+183204_823+183206delinsGAT MANE Select NP_001010848.2:n.823+183204_823+183206del...
NM_001370081.1:c.823+183204_823+183206delinsGAT NP_001357010.1:n.823+183204_823+183206del...
NM_001370082.1:c.79-107360_79-107358delinsGAT NP_001357011.1:n.79-107360_79-107358delin...
NM_001370083.1:c.823+183204_823+183206delinsGAT NP_001357012.1:n.823+183204_823+183206del...
NM_001370084.1:c.823+183204_823+183206delinsGAT NP_001357013.1:n.823+183204_823+183206del...
NR_163251.1:n.971-92036_971-92034delinsGAT
NR_163252.1:n.409+181272_409+181274delinsGAT
NR_163253.1:n.810+169702_810+169704delinsGAT
NM_001165973.2:c.61-107360_61-107358delinsGAT NP_001159445.1:n.61-107360_61-107358delin...