Canonical Allele Identifier: CA342396414

Gene: GJA5

Linked Data

• MyVariant Identifiers: chr1:g.147230941A>G (hg19) ; chr1:g.147758833A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147758833A>G , CM000663.2:g.147758833A>G	GRCh38
NC_000001.10:g.147230941A>G , CM000663.1:g.147230941A>G	GRCh37
NC_000001.9:g.145697565A>G	NCBI36
NG_009369.2:g.19542T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579774.3:c.406T>C MANE Select	ENSP00000463851.1:p.Trp136Arg
ENST00000430508.1:c.406T>C	ENSP00000407645.1:p.Trp136Arg
ENST00000579774.2:c.406T>C	ENSP00000463851.1:p.Trp136Arg
ENST00000621517.1:c.406T>C	ENSP00000484552.1:p.Trp136Arg
NM_005266.6:c.406T>C	NP_005257.2:p.Trp136Arg
NM_181703.3:c.406T>C	NP_859054.1:p.Trp136Arg
XM_005272951.3:c.406T>C	XP_005273008.1:p.Trp136Arg
XM_011509415.1:c.406T>C	XP_011507717.1:p.Trp136Arg
XR_922078.1:n.434-18728A>G
XR_922079.1:n.434-18728A>G
XM_005272951.4:c.406T>C	XP_005273008.1:p.Trp136Arg
XM_017001044.1:c.406T>C	XP_016856533.1:p.Trp136Arg
XR_922079.3:n.744-18728A>G
NM_181703.4:c.406T>C MANE Select	NP_859054.1:p.Trp136Arg
NM_005266.7:c.406T>C	NP_005257.2:p.Trp136Arg