Canonical Allele Identifier: CA1199590017
Gene: GJA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147757672G= , CM000663.2:g.147757672G= GRCh38
NC_000001.10:g.147229780G= , CM000663.1:g.147229780G= GRCh37
NC_000001.9:g.145696404G= NCBI36
NG_009369.2:g.20703C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000579774.3:c.*490C= MANE Select ENSP00000463851.1:n.*490C=
ENST00000579774.2:c.*490C= ENSP00000463851.1:n.*490C=
ENST00000621517.1:c.*490C= ENSP00000484552.1:n.*490C=
NM_005266.6:c.*490C= NP_005257.2:n.*490C=
NM_181703.3:c.*490C= NP_859054.1:n.*490C=
XM_005272951.3:c.*490C= XP_005273008.1:n.*490C=
XM_011509415.1:c.*490C= XP_011507717.1:n.*490C=
XR_922078.1:n.434-19889G=
XR_922079.1:n.434-19889G=
XM_005272951.4:c.*490C= XP_005273008.1:n.*490C=
XM_017001044.1:c.*490C= XP_016856533.1:n.*490C=
XR_922079.3:n.744-19889G=
NM_181703.4:c.*490C= MANE Select NP_859054.1:n.*490C=
NM_005266.7:c.*490C= NP_005257.2:n.*490C=