Canonical Allele Identifier: CA339321799

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794396C>A , CM000663.2:g.34794396C>A GRCh38
NC_000001.10:g.35259997C>A , CM000663.1:g.35259997C>A GRCh37
NC_000001.9:g.35032584C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.183C>A (GJA4) MANE Select ENSP00000343676.4:p.Cys61Ter
ENST00000342280.4:c.183C>A (GJA4) ENSP00000343676.4:p.Cys61Ter
ENST00000426886.1:c.207+61375G>T (SMIM12) ENSP00000429902.1:n.207+61375G>T
ENST00000450137.1:c.183C>A (GJA4) ENSP00000409186.1:p.Cys61Ter
NM_002060.2:c.183C>A (GJA4) NP_002051.2:p.Cys61Ter
XM_005270750.1:c.183C>A (GJA4) XP_005270807.1:p.Cys61Ter
XR_947179.1:n.1001+3975G>T
XM_005270750.2:c.183C>A (GJA4) XP_005270807.1:p.Cys61Ter
XM_017001043.2:c.183C>A (GJA4) XP_016856532.1:p.Cys61Ter
XR_001737967.1:n.1023+3975G>T
NM_002060.3:c.183C>A (GJA4) MANE Select NP_002051.2:p.Cys61Ter