Canonical Allele Identifier: CA420607014
Gene: GJA8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.147380502G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147908375G>A , CM000663.2:g.147908375G>A GRCh38
NC_000001.10:g.147380502G>A , CM000663.1:g.147380502G>A GRCh37
NC_000001.9:g.145847126G>A NCBI36
NG_016242.1:g.10557G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369235.2:c.420G>A MANE Select ENSP00000358238.1:p.Lys140=
ENST00000369235.1:c.420G>A ENSP00000358238.1:p.Lys140=
NM_005267.4:c.420G>A NP_005258.2:p.Lys140=
XM_011509416.1:c.420G>A XP_011507718.1:p.Lys140=
XM_011509417.1:c.420G>A XP_011507719.1:p.Lys140=
XM_011509417.2:c.420G>A XP_011507719.1:p.Lys140=
XR_002956281.1:n.1335G>A
NM_005267.5:c.420G>A MANE Select NP_005258.2:p.Lys140=