Canonical Allele Identifier: CA388465882

Gene: GPC6 GPC6-AS2

Linked Data

• MyVariant Identifiers: chr13:g.94482788G>T (hg19) ; chr13:g.93830535G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830535G>T , CM000675.2:g.93830535G>T	GRCh38
NC_000013.10:g.94482788G>T , CM000675.1:g.94482788G>T	GRCh37
NC_000013.9:g.93280789G>T	NCBI36
NG_011880.1:g.608711G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377047.9:c.701G>T (GPC6) MANE Select	ENSP00000366246.3:p.Arg234Leu
ENST00000377047.8:c.701G>T (GPC6)	ENSP00000366246.3:p.Arg234Leu
NM_005708.3:c.701G>T (GPC6)	NP_005699.1:p.Arg234Leu
NR_046536.1:n.380+281C>A (GPC6-AS2)
XM_011521044.1:c.491G>T (GPC6)	XP_011519346.1:p.Arg164Leu
NM_005708.4:c.701G>T (GPC6)	NP_005699.1:p.Arg234Leu
XM_011521044.2:c.491G>T (GPC6)	XP_011519346.1:p.Arg164Leu
XM_017020298.1:c.491G>T (GPC6)	XP_016875787.1:p.Arg164Leu
XM_017020299.2:c.491G>T (GPC6)	XP_016875788.1:p.Arg164Leu
XM_017020300.1:c.491G>T (GPC6)	XP_016875789.1:p.Arg164Leu
XM_017020301.1:c.335G>T (GPC6)	XP_016875790.1:p.Arg112Leu
NM_005708.5:c.701G>T (GPC6) MANE Select	NP_005699.1:p.Arg234Leu