Canonical Allele Identifier: CA702501658

Gene: GPC6

Linked Data

• dbSNP Id: rs9524260
• MyVariant Identifiers: chr13:g.94513790A>T (hg19) ; chr13:g.93861537A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93861537A>T , CM000675.2:g.93861537A>T	GRCh38
NC_000013.10:g.94513790A>T , CM000675.1:g.94513790A>T	GRCh37
NC_000013.9:g.93311791A>T	NCBI36
NG_011880.1:g.639713A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377047.9:c.711+30992A>T MANE Select	ENSP00000366246.3:n.711+30992A>T
ENST00000377047.8:c.711+30992A>T	ENSP00000366246.3:n.711+30992A>T
NM_005708.3:c.711+30992A>T	NP_005699.1:n.711+30992A>T
XM_011521044.1:c.501+30992A>T	XP_011519346.1:n.501+30992A>T
NM_005708.4:c.711+30992A>T	NP_005699.1:n.711+30992A>T
XM_011521044.2:c.501+30992A>T	XP_011519346.1:n.501+30992A>T
XM_017020298.1:c.501+30992A>T	XP_016875787.1:n.501+30992A>T
XM_017020299.2:c.501+30992A>T	XP_016875788.1:n.501+30992A>T
XM_017020300.1:c.501+30992A>T	XP_016875789.1:n.501+30992A>T
XM_017020301.1:c.345+30992A>T	XP_016875790.1:n.345+30992A>T
NM_005708.5:c.711+30992A>T MANE Select	NP_005699.1:n.711+30992A>T