Canonical Allele Identifier: CA2111284168
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286378T= , CM000675.2:g.93286378T= GRCh38
NC_000013.10:g.93938631T= , CM000675.1:g.93938631T= GRCh37
NC_000013.9:g.92736632T= NCBI36
NG_011880.1:g.64554T=

Transcript Alleles

HGVS Amino-acid change
ENST00000377047.9:c.160+58762T= MANE Select ENSP00000366246.3:n.160+58762T=
ENST00000377047.8:c.160+58762T= ENSP00000366246.3:n.160+58762T=
NM_005708.3:c.160+58762T= NP_005699.1:n.160+58762T=
NM_005708.4:c.160+58762T= NP_005699.1:n.160+58762T=
XM_017020299.2:c.-51+20421T= XP_016875788.1:n.-51+20421T=
NM_005708.5:c.160+58762T= MANE Select NP_005699.1:n.160+58762T=