Canonical Allele Identifier: CA1199591469
Gene: GJA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147759075T= , CM000663.2:g.147759075T= GRCh38
NC_000001.10:g.147231183T= , CM000663.1:g.147231183T= GRCh37
NC_000001.9:g.145697807T= NCBI36
NG_009369.2:g.19300A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000579774.3:c.164A= MANE Select ENSP00000463851.1:p.Asp55=
ENST00000430508.1:c.164A= ENSP00000407645.1:p.Asp55=
ENST00000579774.2:c.164A= ENSP00000463851.1:p.Asp55=
ENST00000621517.1:c.164A= ENSP00000484552.1:p.Asp55=
NM_005266.6:c.164A= NP_005257.2:p.Asp55=
NM_181703.3:c.164A= NP_859054.1:p.Asp55=
XM_005272951.3:c.164A= XP_005273008.1:p.Asp55=
XM_011509415.1:c.164A= XP_011507717.1:p.Asp55=
XR_922078.1:n.434-18486T=
XR_922079.1:n.434-18486T=
XM_005272951.4:c.164A= XP_005273008.1:p.Asp55=
XM_017001044.1:c.164A= XP_016856533.1:p.Asp55=
XR_922079.3:n.744-18486T=
NM_181703.4:c.164A= MANE Select NP_859054.1:p.Asp55=
NM_005266.7:c.164A= NP_005257.2:p.Asp55=