Canonical Allele Identifier: CA342398115
Gene: GJA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147759088C>A , CM000663.2:g.147759088C>A GRCh38
NC_000001.10:g.147231196C>A , CM000663.1:g.147231196C>A GRCh37
NC_000001.9:g.145697820C>A NCBI36
NG_009369.2:g.19287G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000579774.3:c.151G>T MANE Select ENSP00000463851.1:p.Asp51Tyr
ENST00000430508.1:c.151G>T ENSP00000407645.1:p.Asp51Tyr
ENST00000579774.2:c.151G>T ENSP00000463851.1:p.Asp51Tyr
ENST00000621517.1:c.151G>T ENSP00000484552.1:p.Asp51Tyr
NM_005266.6:c.151G>T NP_005257.2:p.Asp51Tyr
NM_181703.3:c.151G>T NP_859054.1:p.Asp51Tyr
XM_005272951.3:c.151G>T XP_005273008.1:p.Asp51Tyr
XM_011509415.1:c.151G>T XP_011507717.1:p.Asp51Tyr
XR_922078.1:n.434-18473C>A
XR_922079.1:n.434-18473C>A
XM_005272951.4:c.151G>T XP_005273008.1:p.Asp51Tyr
XM_017001044.1:c.151G>T XP_016856533.1:p.Asp51Tyr
XR_922079.3:n.744-18473C>A
NM_181703.4:c.151G>T MANE Select NP_859054.1:p.Asp51Tyr
NM_005266.7:c.151G>T NP_005257.2:p.Asp51Tyr