Canonical Allele Identifier: CA2111438262
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93688843G= , CM000675.2:g.93688843G= GRCh38
NC_000013.10:g.94341096G= , CM000675.1:g.94341096G= GRCh37
NC_000013.9:g.93139097G= NCBI36
NG_011880.1:g.467019G=

Transcript Alleles

HGVS Amino-acid Change
NM_005708.5:c.320-141311G= MANE Select NP_005699.1:n.320-141311G=
ENST00000377047.9:c.320-141311G= MANE Select ENSP00000366246.3:n.320-141311G=
NM_005708.3:c.320-141311G= NP_005699.1:n.320-141311G=
NM_005708.4:c.320-141311G= NP_005699.1:n.320-141311G=
ENST00000377047.8:c.320-141311G= ENSP00000366246.3:n.320-141311G=
XM_011521044.1:c.110-141311G= XP_011519346.1:n.110-141311G=
XM_011521044.2:c.110-141311G= XP_011519346.1:n.110-141311G=
XM_017020298.1:c.110-141311G= XP_016875787.1:n.110-141311G=
XM_017020299.2:c.110-141311G= XP_016875788.1:n.110-141311G=
XM_017020300.1:c.110-141311G= XP_016875789.1:n.110-141311G=