Canonical Allele Identifier: CA339323477

Linked Data

gnomAD v4: 1-34794515-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794515G>C , CM000663.2:g.34794515G>C GRCh38
NC_000001.10:g.35260116G>C , CM000663.1:g.35260116G>C GRCh37
NC_000001.9:g.35032703G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.302G>C (GJA4) MANE Select ENSP00000343676.4:p.Arg101Pro
ENST00000342280.4:c.302G>C (GJA4) ENSP00000343676.4:p.Arg101Pro
ENST00000426886.1:c.207+61256C>G (SMIM12) ENSP00000429902.1:n.207+61256C>G
ENST00000450137.1:c.302G>C (GJA4) ENSP00000409186.1:p.Arg101Pro
NM_002060.2:c.302G>C (GJA4) NP_002051.2:p.Arg101Pro
XM_005270750.1:c.302G>C (GJA4) XP_005270807.1:p.Arg101Pro
XR_947179.1:n.1001+3856C>G
XM_005270750.2:c.302G>C (GJA4) XP_005270807.1:p.Arg101Pro
XM_017001043.2:c.302G>C (GJA4) XP_016856532.1:p.Arg101Pro
XR_001737967.1:n.1023+3856C>G
NM_002060.3:c.302G>C (GJA4) MANE Select NP_002051.2:p.Arg101Pro