Canonical Allele Identifier: CA702413247

Gene: GPC6

Linked Data

• dbSNP Id: rs796481386
• MyVariant Identifiers: chr13:g.93938665A>C (hg19) ; chr13:g.93286412A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93286412A>C , CM000675.2:g.93286412A>C	GRCh38
NC_000013.10:g.93938665A>C , CM000675.1:g.93938665A>C	GRCh37
NC_000013.9:g.92736666A>C	NCBI36
NG_011880.1:g.64588A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.160+58796A>C MANE Select	ENSP00000366246.3:n.160+58796A>C
ENST00000377047.8:c.160+58796A>C	ENSP00000366246.3:n.160+58796A>C
NM_005708.3:c.160+58796A>C	NP_005699.1:n.160+58796A>C
NM_005708.4:c.160+58796A>C	NP_005699.1:n.160+58796A>C
XM_017020299.2:c.-51+20455A>C	XP_016875788.1:n.-51+20455A>C
NM_005708.5:c.160+58796A>C MANE Select	NP_005699.1:n.160+58796A>C