Canonical Allele Identifier: CA339320521

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794298C>A , CM000663.2:g.34794298C>A GRCh38
NC_000001.10:g.35259899C>A , CM000663.1:g.35259899C>A GRCh37
NC_000001.9:g.35032486C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.85C>A (GJA4) MANE Select ENSP00000343676.4:p.Leu29Ile
ENST00000342280.4:c.85C>A (GJA4) ENSP00000343676.4:p.Leu29Ile
ENST00000426886.1:c.207+61473G>T (SMIM12) ENSP00000429902.1:n.207+61473G>T
ENST00000450137.1:c.85C>A (GJA4) ENSP00000409186.1:p.Leu29Ile
NM_002060.2:c.85C>A (GJA4) NP_002051.2:p.Leu29Ile
XM_005270750.1:c.85C>A (GJA4) XP_005270807.1:p.Leu29Ile
XR_947179.1:n.1001+4073G>T
XM_005270750.2:c.85C>A (GJA4) XP_005270807.1:p.Leu29Ile
XM_017001043.2:c.85C>A (GJA4) XP_016856532.1:p.Leu29Ile
XR_001737967.1:n.1023+4073G>T
NM_002060.3:c.85C>A (GJA4) MANE Select NP_002051.2:p.Leu29Ile