Canonical Allele Identifier: CA594802958

Gene: NRG3

Linked Data

• dbSNP Id: rs1451243471
• gnomAD v2: 10-84645991-T-C
• MyVariant Identifiers: chr10:g.84645991T>C (hg19) ; chr10:g.82886235T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.82886235T>C , CM000672.2:g.82886235T>C	GRCh38
NC_000010.10:g.84645991T>C , CM000672.1:g.84645991T>C	GRCh37
NC_000010.9:g.84635971T>C	NCBI36
NG_013373.1:g.1015922T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372141.7:c.1054+20798T>C MANE Select	ENSP00000361214.2:n.1054+20798T>C
ENST00000372141.6:c.1054+20798T>C	ENSP00000361214.2:n.1054+20798T>C
ENST00000372142.6:c.391+20798T>C	ENSP00000361215.2:n.391+20798T>C
ENST00000404547.5:c.1054+20798T>C	ENSP00000384796.1:n.1054+20798T>C
ENST00000404576.6:c.466+20798T>C	ENSP00000385804.2:n.466+20798T>C
ENST00000537893.1:c.4+20798T>C	ENSP00000440377.1:n.4+20798T>C
ENST00000545131.5:c.4+20798T>C	ENSP00000441201.1:n.4+20798T>C
ENST00000555784.5:c.454+20798T>C	ENSP00000451858.1:n.454+20798T>C
ENST00000556918.5:c.544+20798T>C	ENSP00000451376.1:n.544+20798T>C
ENST00000602794.5:c.*690+20798T>C	ENSP00000473669.1:n.*690+20798T>C
NM_001010848.3:c.1054+20798T>C	NP_001010848.2:n.1054+20798T>C
NM_001165972.1:c.1051+20798T>C	NP_001159444.1:n.1051+20798T>C
NM_001165973.1:c.391+20798T>C	NP_001159445.1:n.391+20798T>C
XM_005269444.3:c.1054+20798T>C	XP_005269501.1:n.1054+20798T>C
XM_011539172.1:c.1054+20798T>C	XP_011537474.1:n.1054+20798T>C
XM_011539173.1:c.1051+20798T>C	XP_011537475.1:n.1051+20798T>C
XM_011539174.1:c.1028-65234T>C	XP_011537476.1:n.1028-65234T>C
XM_011539175.1:c.1054+20798T>C	XP_011537477.1:n.1054+20798T>C
XM_011539176.1:c.274+20798T>C	XP_011537478.1:n.274+20798T>C
XM_011539177.1:c.274+20798T>C	XP_011537479.1:n.274+20798T>C
XM_011539179.1:c.4+20798T>C	XP_011537481.1:n.4+20798T>C
XM_005269444.5:c.1054+20798T>C	XP_005269501.1:n.1054+20798T>C
XM_011539172.3:c.1054+20798T>C	XP_011537474.1:n.1054+20798T>C
XM_011539173.3:c.1051+20798T>C	XP_011537475.1:n.1051+20798T>C
XM_011539175.3:c.1054+20798T>C	XP_011537477.1:n.1054+20798T>C
XM_017015573.2:c.1132+20798T>C	XP_016871062.1:n.1132+20798T>C
XM_017015574.2:c.1132+20798T>C	XP_016871063.1:n.1132+20798T>C
XM_017015575.2:c.1129+20798T>C	XP_016871064.1:n.1129+20798T>C
XM_017015576.2:c.1129+20798T>C	XP_016871065.1:n.1129+20798T>C
XM_017015577.2:c.1132+20798T>C	XP_016871066.1:n.1132+20798T>C
XM_017015578.2:c.1132+20798T>C	XP_016871067.1:n.1132+20798T>C
XM_017015579.2:c.1129+20798T>C	XP_016871068.1:n.1129+20798T>C
XM_017015580.2:c.1129+20798T>C	XP_016871069.1:n.1129+20798T>C
XM_017015581.2:c.1051+20798T>C	XP_016871070.1:n.1051+20798T>C
XM_017015582.1:c.274+20798T>C	XP_016871071.1:n.274+20798T>C
XM_017015583.1:c.274+20798T>C	XP_016871072.1:n.274+20798T>C
XM_024447781.1:c.4+20798T>C	XP_024303549.1:n.4+20798T>C
XR_001747009.2:n.1283+20798T>C
NM_001010848.4:c.1054+20798T>C MANE Select	NP_001010848.2:n.1054+20798T>C
NM_001370081.1:c.1051+20798T>C	NP_001357010.1:n.1051+20798T>C
NM_001370082.1:c.487+20798T>C	NP_001357011.1:n.487+20798T>C
NM_001370084.1:c.1054+20798T>C	NP_001357013.1:n.1054+20798T>C
NR_163251.1:n.1402+20798T>C
NR_163252.1:n.637+20798T>C
NR_163253.1:n.1129+20798T>C
NM_001165973.2:c.391+20798T>C	NP_001159445.1:n.391+20798T>C