Canonical Allele Identifier: CA388465741

Gene: GPC6 GPC6-AS2

Linked Data

• MyVariant Identifiers: chr13:g.94482719T>A (hg19) ; chr13:g.93830466T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830466T>A , CM000675.2:g.93830466T>A	GRCh38
NC_000013.10:g.94482719T>A , CM000675.1:g.94482719T>A	GRCh37
NC_000013.9:g.93280720T>A	NCBI36
NG_011880.1:g.608642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.632T>A (GPC6) MANE Select	ENSP00000366246.3:p.Val211Asp
ENST00000377047.8:c.632T>A (GPC6)	ENSP00000366246.3:p.Val211Asp
NM_005708.3:c.632T>A (GPC6)	NP_005699.1:p.Val211Asp
NR_046536.1:n.380+350A>T (GPC6-AS2)
XM_011521044.1:c.422T>A (GPC6)	XP_011519346.1:p.Val141Asp
NM_005708.4:c.632T>A (GPC6)	NP_005699.1:p.Val211Asp
XM_011521044.2:c.422T>A (GPC6)	XP_011519346.1:p.Val141Asp
XM_017020298.1:c.422T>A (GPC6)	XP_016875787.1:p.Val141Asp
XM_017020299.2:c.422T>A (GPC6)	XP_016875788.1:p.Val141Asp
XM_017020300.1:c.422T>A (GPC6)	XP_016875789.1:p.Val141Asp
XM_017020301.1:c.266T>A (GPC6)	XP_016875790.1:p.Val89Asp
NM_005708.5:c.632T>A (GPC6) MANE Select	NP_005699.1:p.Val211Asp