Canonical Allele Identifier: CA2111541956

Gene: GPC6 GPC6-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830587T= , CM000675.2:g.93830587T=	GRCh38
NC_000013.10:g.94482840T= , CM000675.1:g.94482840T=	GRCh37
NC_000013.9:g.93280841T=	NCBI36
NG_011880.1:g.608763T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.711+42T= (GPC6) MANE Select	ENSP00000366246.3:n.711+42T=
ENST00000377047.8:c.711+42T= (GPC6)	ENSP00000366246.3:n.711+42T=
NM_005708.3:c.711+42T= (GPC6)	NP_005699.1:n.711+42T=
NR_046536.1:n.380+229A= (GPC6-AS2)
XM_011521044.1:c.501+42T= (GPC6)	XP_011519346.1:n.501+42T=
NM_005708.4:c.711+42T= (GPC6)	NP_005699.1:n.711+42T=
XM_011521044.2:c.501+42T= (GPC6)	XP_011519346.1:n.501+42T=
XM_017020298.1:c.501+42T= (GPC6)	XP_016875787.1:n.501+42T=
XM_017020299.2:c.501+42T= (GPC6)	XP_016875788.1:n.501+42T=
XM_017020300.1:c.501+42T= (GPC6)	XP_016875789.1:n.501+42T=
XM_017020301.1:c.345+42T= (GPC6)	XP_016875790.1:n.345+42T=
NM_005708.5:c.711+42T= (GPC6) MANE Select	NP_005699.1:n.711+42T=