Canonical Allele Identifier: CA2647660359

Gene: GJA5

Linked Data

• gnomAD v4: 1-147757702-AGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147757703_147757705del , CM000663.2:g.147757703_147757705del	GRCh38
NC_000001.10:g.147229811_147229813del , CM000663.1:g.147229811_147229813del	GRCh37
NC_000001.9:g.145696435_145696437del	NCBI36
NG_009369.2:g.20670_20672del

Transcript Alleles

HGVS	Amino-acid change
ENST00000579774.3:c.*457_*459del MANE Select	ENSP00000463851.1:n.*457_*459del
ENST00000579774.2:c.*457_*459del	ENSP00000463851.1:n.*457_*459del
ENST00000621517.1:c.*457_*459del	ENSP00000484552.1:n.*457_*459del
NM_005266.6:c.*457_*459del	NP_005257.2:n.*457_*459del
NM_181703.3:c.*457_*459del	NP_859054.1:n.*457_*459del
XM_005272951.3:c.*457_*459del	XP_005273008.1:n.*457_*459del
XM_011509415.1:c.*457_*459del	XP_011507717.1:n.*457_*459del
XR_922078.1:n.434-19858_434-19856del
XR_922079.1:n.434-19858_434-19856del
XM_005272951.4:c.*457_*459del	XP_005273008.1:n.*457_*459del
XM_017001044.1:c.*457_*459del	XP_016856533.1:n.*457_*459del
XR_922079.3:n.744-19858_744-19856del
NM_181703.4:c.*457_*459del MANE Select	NP_859054.1:n.*457_*459del
NM_005266.7:c.*457_*459del	NP_005257.2:n.*457_*459del