Canonical Allele Identifier: CA1199591242
Gene: GJA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147758905C= , CM000663.2:g.147758905C= GRCh38
NC_000001.10:g.147231013C= , CM000663.1:g.147231013C= GRCh37
NC_000001.9:g.145697637C= NCBI36
NG_009369.2:g.19470G=

Transcript Alleles

HGVS Amino-acid change
ENST00000579774.3:c.334G= MANE Select ENSP00000463851.1:p.Glu112=
ENST00000430508.1:c.334G= ENSP00000407645.1:p.Glu112=
ENST00000579774.2:c.334G= ENSP00000463851.1:p.Glu112=
ENST00000621517.1:c.334G= ENSP00000484552.1:p.Glu112=
NM_005266.6:c.334G= NP_005257.2:p.Glu112=
NM_181703.3:c.334G= NP_859054.1:p.Glu112=
XM_005272951.3:c.334G= XP_005273008.1:p.Glu112=
XM_011509415.1:c.334G= XP_011507717.1:p.Glu112=
XR_922078.1:n.434-18656C=
XR_922079.1:n.434-18656C=
XM_005272951.4:c.334G= XP_005273008.1:p.Glu112=
XM_017001044.1:c.334G= XP_016856533.1:p.Glu112=
XR_922079.3:n.744-18656C=
NM_181703.4:c.334G= MANE Select NP_859054.1:p.Glu112=
NM_005266.7:c.334G= NP_005257.2:p.Glu112=