Canonical Allele Identifier: CA484761727

Gene: GPC6 GPC6-AS2

Linked Data

• gnomAD v4: 13-93830539-T-C
• MyVariant Identifiers: chr13:g.94482792T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830539T>C , CM000675.2:g.93830539T>C	GRCh38
NC_000013.10:g.94482792T>C , CM000675.1:g.94482792T>C	GRCh37
NC_000013.9:g.93280793T>C	NCBI36
NG_011880.1:g.608715T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377047.9:c.705T>C (GPC6) MANE Select	ENSP00000366246.3:p.Val235=
ENST00000377047.8:c.705T>C (GPC6)	ENSP00000366246.3:p.Val235=
NM_005708.3:c.705T>C (GPC6)	NP_005699.1:p.Val235=
NR_046536.1:n.380+277A>G (GPC6-AS2)
XM_011521044.1:c.495T>C (GPC6)	XP_011519346.1:p.Val165=
NM_005708.4:c.705T>C (GPC6)	NP_005699.1:p.Val235=
XM_011521044.2:c.495T>C (GPC6)	XP_011519346.1:p.Val165=
XM_017020298.1:c.495T>C (GPC6)	XP_016875787.1:p.Val165=
XM_017020299.2:c.495T>C (GPC6)	XP_016875788.1:p.Val165=
XM_017020300.1:c.495T>C (GPC6)	XP_016875789.1:p.Val165=
XM_017020301.1:c.339T>C (GPC6)	XP_016875790.1:p.Val113=
NM_005708.5:c.705T>C (GPC6) MANE Select	NP_005699.1:p.Val235=