Canonical Allele Identifier: CA342395339

Gene: GJA5

Linked Data

• MyVariant Identifiers: chr1:g.147230721A>T (hg19) ; chr1:g.147758613A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147758613A>T , CM000663.2:g.147758613A>T	GRCh38
NC_000001.10:g.147230721A>T , CM000663.1:g.147230721A>T	GRCh37
NC_000001.9:g.145697345A>T	NCBI36
NG_009369.2:g.19762T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579774.3:c.626T>A MANE Select	ENSP00000463851.1:p.Val209Asp
ENST00000430508.1:c.626T>A	ENSP00000407645.1:p.Val209Asp
ENST00000579774.2:c.626T>A	ENSP00000463851.1:p.Val209Asp
ENST00000621517.1:c.626T>A	ENSP00000484552.1:p.Val209Asp
NM_005266.6:c.626T>A	NP_005257.2:p.Val209Asp
NM_181703.3:c.626T>A	NP_859054.1:p.Val209Asp
XM_005272951.3:c.626T>A	XP_005273008.1:p.Val209Asp
XM_011509415.1:c.626T>A	XP_011507717.1:p.Val209Asp
XR_922078.1:n.434-18948A>T
XR_922079.1:n.434-18948A>T
XM_005272951.4:c.626T>A	XP_005273008.1:p.Val209Asp
XM_017001044.1:c.626T>A	XP_016856533.1:p.Val209Asp
XR_922079.3:n.744-18948A>T
NM_181703.4:c.626T>A MANE Select	NP_859054.1:p.Val209Asp
NM_005266.7:c.626T>A	NP_005257.2:p.Val209Asp