Canonical Allele Identifier: CA2111694250
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94218537T= , CM000675.2:g.94218537T= GRCh38
NC_000013.10:g.94870791T= , CM000675.1:g.94870791T= GRCh37
NC_000013.9:g.93668792T= NCBI36
NG_011880.1:g.996714T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.878-67812T= MANE Select ENSP00000366246.3:n.878-67812T=
ENST00000377047.8:c.878-67812T= ENSP00000366246.3:n.878-67812T=
NM_005708.3:c.878-67812T= NP_005699.1:n.878-67812T=
XM_011521044.1:c.668-67812T= XP_011519346.1:n.668-67812T=
NM_005708.4:c.878-67812T= NP_005699.1:n.878-67812T=
XM_011521044.2:c.668-67812T= XP_011519346.1:n.668-67812T=
XM_017020298.1:c.668-67812T= XP_016875787.1:n.668-67812T=
XM_017020299.2:c.668-67812T= XP_016875788.1:n.668-67812T=
XM_017020300.1:c.668-67812T= XP_016875789.1:n.668-67812T=
XM_017020301.1:c.512-67812T= XP_016875790.1:n.512-67812T=
XM_017020302.1:c.185-67812T= XP_016875791.1:n.185-67812T=
NM_005708.5:c.878-67812T= MANE Select NP_005699.1:n.878-67812T=