Canonical Allele Identifier: CA1143463029

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794335G= , CM000663.2:g.34794335G= GRCh38
NC_000001.10:g.35259936G= , CM000663.1:g.35259936G= GRCh37
NC_000001.9:g.35032523G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.122G= (GJA4) MANE Select ENSP00000343676.4:p.Gly41=
ENST00000342280.4:c.122G= (GJA4) ENSP00000343676.4:p.Gly41=
ENST00000426886.1:c.207+61436C= (SMIM12) ENSP00000429902.1:n.207+61436C=
ENST00000450137.1:c.122G= (GJA4) ENSP00000409186.1:p.Gly41=
NM_002060.2:c.122G= (GJA4) NP_002051.2:p.Gly41=
XM_005270750.1:c.122G= (GJA4) XP_005270807.1:p.Gly41=
XR_947179.1:n.1001+4036C=
XM_005270750.2:c.122G= (GJA4) XP_005270807.1:p.Gly41=
XM_017001043.2:c.122G= (GJA4) XP_016856532.1:p.Gly41=
XR_001737967.1:n.1023+4036C=
NM_002060.3:c.122G= (GJA4) MANE Select NP_002051.2:p.Gly41=