Canonical Allele Identifier: CA339320619

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794308T>G , CM000663.2:g.34794308T>G GRCh38
NC_000001.10:g.35259909T>G , CM000663.1:g.35259909T>G GRCh37
NC_000001.9:g.35032496T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.95T>G (GJA4) MANE Select ENSP00000343676.4:p.Phe32Cys
ENST00000342280.4:c.95T>G (GJA4) ENSP00000343676.4:p.Phe32Cys
ENST00000426886.1:c.207+61463A>C (SMIM12) ENSP00000429902.1:n.207+61463A>C
ENST00000450137.1:c.95T>G (GJA4) ENSP00000409186.1:p.Phe32Cys
NM_002060.2:c.95T>G (GJA4) NP_002051.2:p.Phe32Cys
XM_005270750.1:c.95T>G (GJA4) XP_005270807.1:p.Phe32Cys
XR_947179.1:n.1001+4063A>C
XM_005270750.2:c.95T>G (GJA4) XP_005270807.1:p.Phe32Cys
XM_017001043.2:c.95T>G (GJA4) XP_016856532.1:p.Phe32Cys
XR_001737967.1:n.1023+4063A>C
NM_002060.3:c.95T>G (GJA4) MANE Select NP_002051.2:p.Phe32Cys