Canonical Allele Identifier: CA339320855

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794332C>A , CM000663.2:g.34794332C>A GRCh38
NC_000001.10:g.35259933C>A , CM000663.1:g.35259933C>A GRCh37
NC_000001.9:g.35032520C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.119C>A (GJA4) MANE Select ENSP00000343676.4:p.Ala40Asp
ENST00000342280.4:c.119C>A (GJA4) ENSP00000343676.4:p.Ala40Asp
ENST00000426886.1:c.207+61439G>T (SMIM12) ENSP00000429902.1:n.207+61439G>T
ENST00000450137.1:c.119C>A (GJA4) ENSP00000409186.1:p.Ala40Asp
NM_002060.2:c.119C>A (GJA4) NP_002051.2:p.Ala40Asp
XM_005270750.1:c.119C>A (GJA4) XP_005270807.1:p.Ala40Asp
XR_947179.1:n.1001+4039G>T
XM_005270750.2:c.119C>A (GJA4) XP_005270807.1:p.Ala40Asp
XM_017001043.2:c.119C>A (GJA4) XP_016856532.1:p.Ala40Asp
XR_001737967.1:n.1023+4039G>T
NM_002060.3:c.119C>A (GJA4) MANE Select NP_002051.2:p.Ala40Asp