Canonical Allele Identifier: CA669013038

Gene: NRG3

Linked Data

• dbSNP Id: rs10883866
• MyVariant Identifiers: chr10:g.83643639C>A (hg19) ; chr10:g.81883883C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.81883883C>A , CM000672.2:g.81883883C>A	GRCh38
NC_000010.10:g.83643639C>A , CM000672.1:g.83643639C>A	GRCh37
NC_000010.9:g.83633619C>A	NCBI36
NG_013373.1:g.13570C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372141.7:c.823+7720C>A MANE Select	ENSP00000361214.2:n.823+7720C>A
ENST00000372141.6:c.823+7720C>A	ENSP00000361214.2:n.823+7720C>A
ENST00000372142.6:c.60+5863C>A	ENSP00000361215.2:n.60+5863C>A
ENST00000404547.5:c.823+7720C>A	ENSP00000384796.1:n.823+7720C>A
ENST00000404576.6:c.135+5788C>A	ENSP00000385804.2:n.135+5788C>A
ENST00000555784.5:c.135+5788C>A	ENSP00000451858.1:n.135+5788C>A
ENST00000556918.5:c.135+5788C>A	ENSP00000451376.1:n.135+5788C>A
ENST00000602794.5:c.61-5307C>A	ENSP00000473669.1:n.61-5307C>A
NM_001010848.3:c.823+7720C>A	NP_001010848.2:n.823+7720C>A
NM_001165972.1:c.823+7720C>A	NP_001159444.1:n.823+7720C>A
NM_001165973.1:c.60+5863C>A	NP_001159445.1:n.60+5863C>A
XM_005269444.3:c.823+7720C>A	XP_005269501.1:n.823+7720C>A
XM_011539172.1:c.823+7720C>A	XP_011537474.1:n.823+7720C>A
XM_011539173.1:c.823+7720C>A	XP_011537475.1:n.823+7720C>A
XM_011539174.1:c.823+7720C>A	XP_011537476.1:n.823+7720C>A
XM_011539175.1:c.823+7720C>A	XP_011537477.1:n.823+7720C>A
XM_005269444.5:c.823+7720C>A	XP_005269501.1:n.823+7720C>A
XM_011539172.3:c.823+7720C>A	XP_011537474.1:n.823+7720C>A
XM_011539173.3:c.823+7720C>A	XP_011537475.1:n.823+7720C>A
XM_011539175.3:c.823+7720C>A	XP_011537477.1:n.823+7720C>A
XM_017015573.2:c.823+7720C>A	XP_016871062.1:n.823+7720C>A
XM_017015574.2:c.823+7720C>A	XP_016871063.1:n.823+7720C>A
XM_017015575.2:c.823+7720C>A	XP_016871064.1:n.823+7720C>A
XM_017015576.2:c.823+7720C>A	XP_016871065.1:n.823+7720C>A
XM_017015577.2:c.823+7720C>A	XP_016871066.1:n.823+7720C>A
XM_017015578.2:c.823+7720C>A	XP_016871067.1:n.823+7720C>A
XM_017015579.2:c.823+7720C>A	XP_016871068.1:n.823+7720C>A
XM_017015580.2:c.823+7720C>A	XP_016871069.1:n.823+7720C>A
XM_017015581.2:c.823+7720C>A	XP_016871070.1:n.823+7720C>A
XM_017015584.2:c.823+7720C>A	XP_016871073.1:n.823+7720C>A
XR_001747009.2:n.974+7720C>A
NM_001010848.4:c.823+7720C>A MANE Select	NP_001010848.2:n.823+7720C>A
NM_001370081.1:c.823+7720C>A	NP_001357010.1:n.823+7720C>A
NM_001370082.1:c.78+7720C>A	NP_001357011.1:n.78+7720C>A
NM_001370083.1:c.823+7720C>A	NP_001357012.1:n.823+7720C>A
NM_001370084.1:c.823+7720C>A	NP_001357013.1:n.823+7720C>A
NR_163251.1:n.970+7720C>A
NR_163252.1:n.409+5788C>A
NR_163253.1:n.335-5307C>A
NM_001165973.2:c.60+5863C>A	NP_001159445.1:n.60+5863C>A