Canonical Allele Identifier: CA1199590047
Gene: GJA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147757709T= , CM000663.2:g.147757709T= GRCh38
NC_000001.10:g.147229817T= , CM000663.1:g.147229817T= GRCh37
NC_000001.9:g.145696441T= NCBI36
NG_009369.2:g.20666A=

Transcript Alleles

HGVS Amino-acid change
ENST00000579774.3:c.*453A= MANE Select ENSP00000463851.1:n.*453A=
ENST00000579774.2:c.*453A= ENSP00000463851.1:n.*453A=
ENST00000621517.1:c.*453A= ENSP00000484552.1:n.*453A=
NM_005266.6:c.*453A= NP_005257.2:n.*453A=
NM_181703.3:c.*453A= NP_859054.1:n.*453A=
XM_005272951.3:c.*453A= XP_005273008.1:n.*453A=
XM_011509415.1:c.*453A= XP_011507717.1:n.*453A=
XR_922078.1:n.434-19852T=
XR_922079.1:n.434-19852T=
XM_005272951.4:c.*453A= XP_005273008.1:n.*453A=
XM_017001044.1:c.*453A= XP_016856533.1:n.*453A=
XR_922079.3:n.744-19852T=
NM_181703.4:c.*453A= MANE Select NP_859054.1:n.*453A=
NM_005266.7:c.*453A= NP_005257.2:n.*453A=