Canonical Allele Identifier: CA2800185281

Gene: GPC6 GPC6-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830623_93830624insCC , CM000675.2:g.93830623_93830624insCC	GRCh38
NC_000013.10:g.94482876_94482877insCC , CM000675.1:g.94482876_94482877insCC	GRCh37
NC_000013.9:g.93280877_93280878insCC	NCBI36
NG_011880.1:g.608799_608800insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.711+78_711+79insCC (GPC6) MANE Select	ENSP00000366246.3:n.711+78_711+79insCC
ENST00000377047.8:c.711+78_711+79insCC (GPC6)	ENSP00000366246.3:n.711+78_711+79insCC
NM_005708.3:c.711+78_711+79insCC (GPC6)	NP_005699.1:n.711+78_711+79insCC
NR_046536.1:n.380+192_380+193insGG (GPC6-AS2)
XM_011521044.1:c.501+78_501+79insCC (GPC6)	XP_011519346.1:n.501+78_501+79insCC
NM_005708.4:c.711+78_711+79insCC (GPC6)	NP_005699.1:n.711+78_711+79insCC
XM_011521044.2:c.501+78_501+79insCC (GPC6)	XP_011519346.1:n.501+78_501+79insCC
XM_017020298.1:c.501+78_501+79insCC (GPC6)	XP_016875787.1:n.501+78_501+79insCC
XM_017020299.2:c.501+78_501+79insCC (GPC6)	XP_016875788.1:n.501+78_501+79insCC
XM_017020300.1:c.501+78_501+79insCC (GPC6)	XP_016875789.1:n.501+78_501+79insCC
XM_017020301.1:c.345+78_345+79insCC (GPC6)	XP_016875790.1:n.345+78_345+79insCC
NM_005708.5:c.711+78_711+79insCC (GPC6) MANE Select	NP_005699.1:n.711+78_711+79insCC