Canonical Allele Identifier: CA339321965

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794410A>T , CM000663.2:g.34794410A>T GRCh38
NC_000001.10:g.35260011A>T , CM000663.1:g.35260011A>T GRCh37
NC_000001.9:g.35032598A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.197A>T (GJA4) MANE Select ENSP00000343676.4:p.Tyr66Phe
ENST00000342280.4:c.197A>T (GJA4) ENSP00000343676.4:p.Tyr66Phe
ENST00000426886.1:c.207+61361T>A (SMIM12) ENSP00000429902.1:n.207+61361T>A
ENST00000450137.1:c.197A>T (GJA4) ENSP00000409186.1:p.Tyr66Phe
NM_002060.2:c.197A>T (GJA4) NP_002051.2:p.Tyr66Phe
XM_005270750.1:c.197A>T (GJA4) XP_005270807.1:p.Tyr66Phe
XR_947179.1:n.1001+3961T>A
XM_005270750.2:c.197A>T (GJA4) XP_005270807.1:p.Tyr66Phe
XM_017001043.2:c.197A>T (GJA4) XP_016856532.1:p.Tyr66Phe
XR_001737967.1:n.1023+3961T>A
NM_002060.3:c.197A>T (GJA4) MANE Select NP_002051.2:p.Tyr66Phe