Canonical Allele Identifier: CA2623380700

Gene: GPC6 GPC6-AS2

Linked Data

• gnomAD v4: 13-93830611-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93830612_93830613del , CM000675.2:g.93830612_93830613del	GRCh38
NC_000013.10:g.94482865_94482866del , CM000675.1:g.94482865_94482866del	GRCh37
NC_000013.9:g.93280866_93280867del	NCBI36
NG_011880.1:g.608788_608789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.711+67_711+68del (GPC6) MANE Select	ENSP00000366246.3:n.711+67_711+68del
ENST00000377047.8:c.711+67_711+68del (GPC6)	ENSP00000366246.3:n.711+67_711+68del
NM_005708.3:c.711+67_711+68del (GPC6)	NP_005699.1:n.711+67_711+68del
NR_046536.1:n.380+203_380+204del (GPC6-AS2)
XM_011521044.1:c.501+67_501+68del (GPC6)	XP_011519346.1:n.501+67_501+68del
NM_005708.4:c.711+67_711+68del (GPC6)	NP_005699.1:n.711+67_711+68del
XM_011521044.2:c.501+67_501+68del (GPC6)	XP_011519346.1:n.501+67_501+68del
XM_017020298.1:c.501+67_501+68del (GPC6)	XP_016875787.1:n.501+67_501+68del
XM_017020299.2:c.501+67_501+68del (GPC6)	XP_016875788.1:n.501+67_501+68del
XM_017020300.1:c.501+67_501+68del (GPC6)	XP_016875789.1:n.501+67_501+68del
XM_017020301.1:c.345+67_345+68del (GPC6)	XP_016875790.1:n.345+67_345+68del
NM_005708.5:c.711+67_711+68del (GPC6) MANE Select	NP_005699.1:n.711+67_711+68del