Canonical Allele Identifier: CA7016933
Gene: GPC6 HGNC NCBI
GPC6-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93830638dup , CM000675.2:g.93830638dup GRCh38
NC_000013.10:g.94482891dup , CM000675.1:g.94482891dup GRCh37
NC_000013.9:g.93280892dup NCBI36
NG_011880.1:g.608814dup

Transcript Alleles

HGVS Amino-acid Change
NM_005708.5:c.711+93dup (GPC6) MANE Select NP_005699.1:n.711+93dup
ENST00000377047.9:c.711+93dup (GPC6) MANE Select ENSP00000366246.3:n.711+93dup
NM_005708.3:c.711+93dup (GPC6) NP_005699.1:n.711+93dup
NM_005708.4:c.711+93dup (GPC6) NP_005699.1:n.711+93dup
NR_046536.1:n.380+203dup (GPC6-AS2)
ENST00000377047.8:c.711+93dup (GPC6) ENSP00000366246.3:n.711+93dup
XM_011521044.1:c.501+93dup (GPC6) XP_011519346.1:n.501+93dup
XM_011521044.2:c.501+93dup (GPC6) XP_011519346.1:n.501+93dup
XM_017020298.1:c.501+93dup (GPC6) XP_016875787.1:n.501+93dup
XM_017020299.2:c.501+93dup (GPC6) XP_016875788.1:n.501+93dup
XM_017020300.1:c.501+93dup (GPC6) XP_016875789.1:n.501+93dup
XM_017020301.1:c.345+93dup (GPC6) XP_016875790.1:n.345+93dup