Canonical Allele Identifier: CA342396263

Gene: GJA5

Linked Data

• MyVariant Identifiers: chr1:g.147230919A>G (hg19) ; chr1:g.147758811A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147758811A>G , CM000663.2:g.147758811A>G	GRCh38
NC_000001.10:g.147230919A>G , CM000663.1:g.147230919A>G	GRCh37
NC_000001.9:g.145697543A>G	NCBI36
NG_009369.2:g.19564T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000579774.3:c.428T>C MANE Select	ENSP00000463851.1:p.Ile143Thr
ENST00000430508.1:c.428T>C	ENSP00000407645.1:p.Ile143Thr
ENST00000579774.2:c.428T>C	ENSP00000463851.1:p.Ile143Thr
ENST00000621517.1:c.428T>C	ENSP00000484552.1:p.Ile143Thr
NM_005266.6:c.428T>C	NP_005257.2:p.Ile143Thr
NM_181703.3:c.428T>C	NP_859054.1:p.Ile143Thr
XM_005272951.3:c.428T>C	XP_005273008.1:p.Ile143Thr
XM_011509415.1:c.428T>C	XP_011507717.1:p.Ile143Thr
XR_922078.1:n.434-18750A>G
XR_922079.1:n.434-18750A>G
XM_005272951.4:c.428T>C	XP_005273008.1:p.Ile143Thr
XM_017001044.1:c.428T>C	XP_016856533.1:p.Ile143Thr
XR_922079.3:n.744-18750A>G
NM_181703.4:c.428T>C MANE Select	NP_859054.1:p.Ile143Thr
NM_005266.7:c.428T>C	NP_005257.2:p.Ile143Thr