Canonical Allele Identifier: CA484761713

Gene: GPC6 GPC6-AS2

Linked Data

• MyVariant Identifiers: chr13:g.94482771C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830518C>T , CM000675.2:g.93830518C>T	GRCh38
NC_000013.10:g.94482771C>T , CM000675.1:g.94482771C>T	GRCh37
NC_000013.9:g.93280772C>T	NCBI36
NG_011880.1:g.608694C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.684C>T (GPC6) MANE Select	ENSP00000366246.3:p.Gly228=
ENST00000377047.8:c.684C>T (GPC6)	ENSP00000366246.3:p.Gly228=
NM_005708.3:c.684C>T (GPC6)	NP_005699.1:p.Gly228=
NR_046536.1:n.380+298G>A (GPC6-AS2)
XM_011521044.1:c.474C>T (GPC6)	XP_011519346.1:p.Gly158=
NM_005708.4:c.684C>T (GPC6)	NP_005699.1:p.Gly228=
XM_011521044.2:c.474C>T (GPC6)	XP_011519346.1:p.Gly158=
XM_017020298.1:c.474C>T (GPC6)	XP_016875787.1:p.Gly158=
XM_017020299.2:c.474C>T (GPC6)	XP_016875788.1:p.Gly158=
XM_017020300.1:c.474C>T (GPC6)	XP_016875789.1:p.Gly158=
XM_017020301.1:c.318C>T (GPC6)	XP_016875790.1:p.Gly106=
NM_005708.5:c.684C>T (GPC6) MANE Select	NP_005699.1:p.Gly228=