Canonical Allele Identifier: CA755025

Linked Data

dbSNP Id: rs765204798

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794531del , CM000663.2:g.34794531del GRCh38
NC_000001.10:g.35260132del , CM000663.1:g.35260132del GRCh37
NC_000001.9:g.35032719del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.318del (GJA4) MANE Select ENSP00000343676.4:p.Arg107GlyfsTer24
ENST00000342280.4:c.318del (GJA4) ENSP00000343676.4:p.Arg107GlyfsTer24
ENST00000426886.1:c.207+61240del (SMIM12) ENSP00000429902.1:n.207+61240del
ENST00000450137.1:c.318del (GJA4) ENSP00000409186.1:p.Arg107GlyfsTer24
NM_002060.2:c.318del (GJA4) NP_002051.2:p.Arg107GlyfsTer24
XM_005270750.1:c.318del (GJA4) XP_005270807.1:p.Arg107GlyfsTer24
XR_947179.1:n.1001+3840del
XM_005270750.2:c.318del (GJA4) XP_005270807.1:p.Arg107GlyfsTer24
XM_017001043.2:c.318del (GJA4) XP_016856532.1:p.Arg107GlyfsTer24
XR_001737967.1:n.1023+3840del
NM_002060.3:c.318del (GJA4) MANE Select NP_002051.2:p.Arg107GlyfsTer24