Canonical Allele Identifier: CA339322640

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794457T>G , CM000663.2:g.34794457T>G GRCh38
NC_000001.10:g.35260058T>G , CM000663.1:g.35260058T>G GRCh37
NC_000001.9:g.35032645T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.244T>G (GJA4) MANE Select ENSP00000343676.4:p.Phe82Val
ENST00000342280.4:c.244T>G (GJA4) ENSP00000343676.4:p.Phe82Val
ENST00000426886.1:c.207+61314A>C (SMIM12) ENSP00000429902.1:n.207+61314A>C
ENST00000450137.1:c.244T>G (GJA4) ENSP00000409186.1:p.Phe82Val
NM_002060.2:c.244T>G (GJA4) NP_002051.2:p.Phe82Val
XM_005270750.1:c.244T>G (GJA4) XP_005270807.1:p.Phe82Val
XR_947179.1:n.1001+3914A>C
XM_005270750.2:c.244T>G (GJA4) XP_005270807.1:p.Phe82Val
XM_017001043.2:c.244T>G (GJA4) XP_016856532.1:p.Phe82Val
XR_001737967.1:n.1023+3914A>C
NM_002060.3:c.244T>G (GJA4) MANE Select NP_002051.2:p.Phe82Val