Canonical Allele Identifier: CA2644771115

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794123_34794124del , CM000663.2:g.34794123_34794124del GRCh38
NC_000001.10:g.35259724_35259725del , CM000663.1:g.35259724_35259725del GRCh37
NC_000001.9:g.35032311_35032312del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.-17-74_-17-73del (GJA4) MANE Select ENSP00000343676.4:n.-17-74_-17-73del
ENST00000342280.4:c.-17-74_-17-73del (GJA4) ENSP00000343676.4:n.-17-74_-17-73del
ENST00000426886.1:c.207+61648_207+61649del (SMIM12) ENSP00000429902.1:n.207+61648_207+61649del
ENST00000450137.1:c.-91_-90del (GJA4) ENSP00000409186.1:n.-91_-90del
NM_002060.2:c.-17-74_-17-73del (GJA4) NP_002051.2:n.-17-74_-17-73del
XM_005270750.1:c.-91_-90del (GJA4) XP_005270807.1:n.-91_-90del
XR_947179.1:n.1001+4248_1001+4249del
XM_005270750.2:c.-91_-90del (GJA4) XP_005270807.1:n.-91_-90del
XM_017001043.2:c.-17-74_-17-73del (GJA4) XP_016856532.1:n.-17-74_-17-73del
XR_001737967.1:n.1023+4248_1023+4249del
NM_002060.3:c.-17-74_-17-73del (GJA4) MANE Select NP_002051.2:n.-17-74_-17-73del