Canonical Allele Identifier: CA2111450893
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93756253A>T , CM000675.2:g.93756253A>T GRCh38
NC_000013.10:g.94408506A>T , CM000675.1:g.94408506A>T GRCh37
NC_000013.9:g.93206507A>T NCBI36
NG_011880.1:g.534429A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.320-73901A>T MANE Select ENSP00000366246.3:n.320-73901A>T
ENST00000377047.8:c.320-73901A>T ENSP00000366246.3:n.320-73901A>T
NM_005708.3:c.320-73901A>T NP_005699.1:n.320-73901A>T
XM_011521044.1:c.110-73901A>T XP_011519346.1:n.110-73901A>T
NM_005708.4:c.320-73901A>T NP_005699.1:n.320-73901A>T
XM_011521044.2:c.110-73901A>T XP_011519346.1:n.110-73901A>T
XM_017020298.1:c.110-73901A>T XP_016875787.1:n.110-73901A>T
XM_017020299.2:c.110-73901A>T XP_016875788.1:n.110-73901A>T
XM_017020300.1:c.110-73901A>T XP_016875789.1:n.110-73901A>T
NM_005708.5:c.320-73901A>T MANE Select NP_005699.1:n.320-73901A>T