Canonical Allele Identifier: CA1199652792
Gene: GJA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147908401G= , CM000663.2:g.147908401G= GRCh38
NC_000001.10:g.147380528G= , CM000663.1:g.147380528G= GRCh37
NC_000001.9:g.145847152G= NCBI36
NG_016242.1:g.10583G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.446G= MANE Select ENSP00000358238.1:p.Arg149=
ENST00000369235.1:c.446G= ENSP00000358238.1:p.Arg149=
NM_005267.4:c.446G= NP_005258.2:p.Arg149=
XM_011509416.1:c.446G= XP_011507718.1:p.Arg149=
XM_011509417.1:c.446G= XP_011507719.1:p.Arg149=
XM_011509417.2:c.446G= XP_011507719.1:p.Arg149=
XR_002956281.1:n.1361G=
NM_005267.5:c.446G= MANE Select NP_005258.2:p.Arg149=