Canonical Allele Identifier: CA2535888502
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286385A>G , CM000675.2:g.93286385A>G GRCh38
NC_000013.10:g.93938638A>G , CM000675.1:g.93938638A>G GRCh37
NC_000013.9:g.92736639A>G NCBI36
NG_011880.1:g.64561A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.160+58769A>G MANE Select ENSP00000366246.3:n.160+58769A>G
ENST00000377047.8:c.160+58769A>G ENSP00000366246.3:n.160+58769A>G
NM_005708.3:c.160+58769A>G NP_005699.1:n.160+58769A>G
NM_005708.4:c.160+58769A>G NP_005699.1:n.160+58769A>G
XM_017020299.2:c.-51+20428A>G XP_016875788.1:n.-51+20428A>G
NM_005708.5:c.160+58769A>G MANE Select NP_005699.1:n.160+58769A>G