Canonical Allele Identifier: CA2573892732
Gene: GJA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147758594dup , CM000663.2:g.147758594dup GRCh38
NC_000001.10:g.147230702dup , CM000663.1:g.147230702dup GRCh37
NC_000001.9:g.145697326dup NCBI36
NG_009369.2:g.19781dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000579774.3:c.645dup MANE Select ENSP00000463851.1:p.Ala216CysfsTer7
ENST00000430508.1:c.645dup ENSP00000407645.1:p.Ala216CysfsTer7
ENST00000579774.2:c.645dup ENSP00000463851.1:p.Ala216CysfsTer7
ENST00000621517.1:c.645dup ENSP00000484552.1:p.Ala216CysfsTer7
NM_005266.6:c.645dup NP_005257.2:p.Ala216CysfsTer7
NM_181703.3:c.645dup NP_859054.1:p.Ala216CysfsTer7
XM_005272951.3:c.645dup XP_005273008.1:p.Ala216CysfsTer7
XM_011509415.1:c.645dup XP_011507717.1:p.Ala216CysfsTer7
XR_922078.1:n.434-18967dup
XR_922079.1:n.434-18967dup
XM_005272951.4:c.645dup XP_005273008.1:p.Ala216CysfsTer7
XM_017001044.1:c.645dup XP_016856533.1:p.Ala216CysfsTer7
XR_922079.3:n.744-18967dup
NM_181703.4:c.645dup MANE Select NP_859054.1:p.Ala216CysfsTer7
NM_005266.7:c.645dup NP_005257.2:p.Ala216CysfsTer7