Canonical Allele Identifier: CA702561202

Gene: GPC6

Linked Data

• dbSNP Id: rs1251206280
• MyVariant Identifiers: chr13:g.94870601C>A (hg19) ; chr13:g.94218347C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94218347C>A , CM000675.2:g.94218347C>A	GRCh38
NC_000013.10:g.94870601C>A , CM000675.1:g.94870601C>A	GRCh37
NC_000013.9:g.93668602C>A	NCBI36
NG_011880.1:g.996524C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.878-68002C>A MANE Select	ENSP00000366246.3:n.878-68002C>A
ENST00000377047.8:c.878-68002C>A	ENSP00000366246.3:n.878-68002C>A
NM_005708.3:c.878-68002C>A	NP_005699.1:n.878-68002C>A
XM_011521044.1:c.668-68002C>A	XP_011519346.1:n.668-68002C>A
NM_005708.4:c.878-68002C>A	NP_005699.1:n.878-68002C>A
XM_011521044.2:c.668-68002C>A	XP_011519346.1:n.668-68002C>A
XM_017020298.1:c.668-68002C>A	XP_016875787.1:n.668-68002C>A
XM_017020299.2:c.668-68002C>A	XP_016875788.1:n.668-68002C>A
XM_017020300.1:c.668-68002C>A	XP_016875789.1:n.668-68002C>A
XM_017020301.1:c.512-68002C>A	XP_016875790.1:n.512-68002C>A
XM_017020302.1:c.185-68002C>A	XP_016875791.1:n.185-68002C>A
NM_005708.5:c.878-68002C>A MANE Select	NP_005699.1:n.878-68002C>A