Canonical Allele Identifier: CA2111284162
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286355G= , CM000675.2:g.93286355G= GRCh38
NC_000013.10:g.93938608G= , CM000675.1:g.93938608G= GRCh37
NC_000013.9:g.92736609G= NCBI36
NG_011880.1:g.64531G=

Transcript Alleles

HGVS Amino-acid change
ENST00000377047.9:c.160+58739G= MANE Select ENSP00000366246.3:n.160+58739G=
ENST00000377047.8:c.160+58739G= ENSP00000366246.3:n.160+58739G=
NM_005708.3:c.160+58739G= NP_005699.1:n.160+58739G=
NM_005708.4:c.160+58739G= NP_005699.1:n.160+58739G=
XM_017020299.2:c.-51+20398G= XP_016875788.1:n.-51+20398G=
NM_005708.5:c.160+58739G= MANE Select NP_005699.1:n.160+58739G=