Canonical Allele Identifier: CA1199652729
Gene: GJA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147908276A= , CM000663.2:g.147908276A= GRCh38
NC_000001.10:g.147380403A= , CM000663.1:g.147380403A= GRCh37
NC_000001.9:g.145847027A= NCBI36
NG_016242.1:g.10458A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.321A= MANE Select ENSP00000358238.1:p.Lys107=
ENST00000369235.1:c.321A= ENSP00000358238.1:p.Lys107=
NM_005267.4:c.321A= NP_005258.2:p.Lys107=
XM_011509416.1:c.321A= XP_011507718.1:p.Lys107=
XM_011509417.1:c.321A= XP_011507719.1:p.Lys107=
XM_011509417.2:c.321A= XP_011507719.1:p.Lys107=
XR_002956281.1:n.1236A=
NM_005267.5:c.321A= MANE Select NP_005258.2:p.Lys107=