Canonical Allele Identifier: CA388465907

Gene: GPC6 GPC6-AS2

Linked Data

• MyVariant Identifiers: chr13:g.94482800T>G (hg19) ; chr13:g.93830547T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830547T>G , CM000675.2:g.93830547T>G	GRCh38
NC_000013.10:g.94482800T>G , CM000675.1:g.94482800T>G	GRCh37
NC_000013.9:g.93280801T>G	NCBI36
NG_011880.1:g.608723T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377047.9:c.711+2T>G (GPC6) MANE Select	ENSP00000366246.3:n.711+2T>G
ENST00000377047.8:c.711+2T>G (GPC6)	ENSP00000366246.3:n.711+2T>G
NM_005708.3:c.711+2T>G (GPC6)	NP_005699.1:n.711+2T>G
NR_046536.1:n.380+269A>C (GPC6-AS2)
XM_011521044.1:c.501+2T>G (GPC6)	XP_011519346.1:n.501+2T>G
NM_005708.4:c.711+2T>G (GPC6)	NP_005699.1:n.711+2T>G
XM_011521044.2:c.501+2T>G (GPC6)	XP_011519346.1:n.501+2T>G
XM_017020298.1:c.501+2T>G (GPC6)	XP_016875787.1:n.501+2T>G
XM_017020299.2:c.501+2T>G (GPC6)	XP_016875788.1:n.501+2T>G
XM_017020300.1:c.501+2T>G (GPC6)	XP_016875789.1:n.501+2T>G
XM_017020301.1:c.345+2T>G (GPC6)	XP_016875790.1:n.345+2T>G
NM_005708.5:c.711+2T>G (GPC6) MANE Select	NP_005699.1:n.711+2T>G