Canonical Allele Identifier: CA1162037198

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34795167_34795168delinsAC , CM000663.2:g.34795167_34795168delinsAC GRCh38
NC_000001.10:g.35260768_35260769delinsAC , CM000663.1:g.35260768_35260769delinsAC GRCh37
NC_000001.9:g.35033355_35033356delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000342280.5:c.954_955delinsAC (GJA4) MANE Select ENSP00000343676.4:p.Lys318=
ENST00000342280.4:c.954_955delinsAC (GJA4) ENSP00000343676.4:p.Lys318=
ENST00000426886.1:c.207+60603_207+60604delinsGT (SMIM12) ENSP00000429902.1:n.207+60603_207+60604de...
NM_002060.2:c.954_955delinsAC (GJA4) NP_002051.2:p.Lys318=
XM_005270750.1:c.954_955delinsAC (GJA4) XP_005270807.1:p.Lys318=
XR_947179.1:n.1001+3203_1001+3204delinsGT
XM_005270750.2:c.954_955delinsAC (GJA4) XP_005270807.1:p.Lys318=
XM_017001043.2:c.954_955delinsAC (GJA4) XP_016856532.1:p.Lys318=
XR_001737967.1:n.1023+3203_1023+3204delinsGT
NM_002060.3:c.954_955delinsAC (GJA4) MANE Select NP_002051.2:p.Lys318=