Canonical Allele Identifier: CA342396211

Gene: GJA5

Linked Data

• MyVariant Identifiers: chr1:g.147230905T>C (hg19) ; chr1:g.147758797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147758797T>C , CM000663.2:g.147758797T>C	GRCh38
NC_000001.10:g.147230905T>C , CM000663.1:g.147230905T>C	GRCh37
NC_000001.9:g.145697529T>C	NCBI36
NG_009369.2:g.19578A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000579774.3:c.442A>G MANE Select	ENSP00000463851.1:p.Thr148Ala
ENST00000430508.1:c.442A>G	ENSP00000407645.1:p.Thr148Ala
ENST00000579774.2:c.442A>G	ENSP00000463851.1:p.Thr148Ala
ENST00000621517.1:c.442A>G	ENSP00000484552.1:p.Thr148Ala
NM_005266.6:c.442A>G	NP_005257.2:p.Thr148Ala
NM_181703.3:c.442A>G	NP_859054.1:p.Thr148Ala
XM_005272951.3:c.442A>G	XP_005273008.1:p.Thr148Ala
XM_011509415.1:c.442A>G	XP_011507717.1:p.Thr148Ala
XR_922078.1:n.434-18764T>C
XR_922079.1:n.434-18764T>C
XM_005272951.4:c.442A>G	XP_005273008.1:p.Thr148Ala
XM_017001044.1:c.442A>G	XP_016856533.1:p.Thr148Ala
XR_922079.3:n.744-18764T>C
NM_181703.4:c.442A>G MANE Select	NP_859054.1:p.Thr148Ala
NM_005266.7:c.442A>G	NP_005257.2:p.Thr148Ala