Canonical Allele Identifier: CA2644771131

Linked Data

gnomAD v4: 1-34794135-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794135T>C , CM000663.2:g.34794135T>C GRCh38
NC_000001.10:g.35259736T>C , CM000663.1:g.35259736T>C GRCh37
NC_000001.9:g.35032323T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.-17-62T>C (GJA4) MANE Select ENSP00000343676.4:n.-17-62T>C
ENST00000342280.4:c.-17-62T>C (GJA4) ENSP00000343676.4:n.-17-62T>C
ENST00000426886.1:c.207+61636A>G (SMIM12) ENSP00000429902.1:n.207+61636A>G
ENST00000450137.1:c.-79T>C (GJA4) ENSP00000409186.1:n.-79T>C
NM_002060.2:c.-17-62T>C (GJA4) NP_002051.2:n.-17-62T>C
XM_005270750.1:c.-79T>C (GJA4) XP_005270807.1:n.-79T>C
XR_947179.1:n.1001+4236A>G
XM_005270750.2:c.-79T>C (GJA4) XP_005270807.1:n.-79T>C
XM_017001043.2:c.-17-62T>C (GJA4) XP_016856532.1:n.-17-62T>C
XR_001737967.1:n.1023+4236A>G
NM_002060.3:c.-17-62T>C (GJA4) MANE Select NP_002051.2:n.-17-62T>C