Canonical Allele Identifier: CA10608082

Gene: GJA5

Linked Data

• dbSNP Id: rs11267274
• MyVariant Identifiers: chr1:g.147757521_147757545dup25 (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147757521_147757545dup , CM000663.2:g.147757521_147757545dup	GRCh38
NG_009369.2:g.20855_20879dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000579774.3:c.*642_*666dup MANE Select	ENSP00000463851.1:n.*642_*666dup
ENST00000579774.2:c.*642_*666dup	ENSP00000463851.1:n.*642_*666dup
ENST00000621517.1:c.*642_*666dup	ENSP00000484552.1:n.*642_*666dup
NM_005266.6:c.*642_*666dup	NP_005257.2:n.*642_*666dup
NM_181703.3:c.*642_*666dup	NP_859054.1:n.*642_*666dup
XM_005272951.3:c.*642_*666dup	XP_005273008.1:n.*642_*666dup
XM_011509415.1:c.*642_*666dup	XP_011507717.1:n.*642_*666dup
XR_922078.1:n.434-20040_434-20016dup
XR_922079.1:n.434-20040_434-20016dup
XM_005272951.4:c.*642_*666dup	XP_005273008.1:n.*642_*666dup
XM_017001044.1:c.*642_*666dup	XP_016856533.1:n.*642_*666dup
XR_922079.3:n.744-20040_744-20016dup
NM_181703.4:c.*642_*666dup MANE Select	NP_859054.1:n.*642_*666dup
NM_005266.7:c.*642_*666dup	NP_005257.2:n.*642_*666dup