Canonical Allele Identifier: CA2623380694

Gene: GPC6 GPC6-AS2

Linked Data

• gnomAD v4: 13-93830610-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830610T>A , CM000675.2:g.93830610T>A	GRCh38
NC_000013.10:g.94482863T>A , CM000675.1:g.94482863T>A	GRCh37
NC_000013.9:g.93280864T>A	NCBI36
NG_011880.1:g.608786T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.711+65T>A (GPC6) MANE Select	ENSP00000366246.3:n.711+65T>A
ENST00000377047.8:c.711+65T>A (GPC6)	ENSP00000366246.3:n.711+65T>A
NM_005708.3:c.711+65T>A (GPC6)	NP_005699.1:n.711+65T>A
NR_046536.1:n.380+206A>T (GPC6-AS2)
XM_011521044.1:c.501+65T>A (GPC6)	XP_011519346.1:n.501+65T>A
NM_005708.4:c.711+65T>A (GPC6)	NP_005699.1:n.711+65T>A
XM_011521044.2:c.501+65T>A (GPC6)	XP_011519346.1:n.501+65T>A
XM_017020298.1:c.501+65T>A (GPC6)	XP_016875787.1:n.501+65T>A
XM_017020299.2:c.501+65T>A (GPC6)	XP_016875788.1:n.501+65T>A
XM_017020300.1:c.501+65T>A (GPC6)	XP_016875789.1:n.501+65T>A
XM_017020301.1:c.345+65T>A (GPC6)	XP_016875790.1:n.345+65T>A
NM_005708.5:c.711+65T>A (GPC6) MANE Select	NP_005699.1:n.711+65T>A