Canonical Allele Identifier: CA342223786

Gene: GJA8

Linked Data

• MyVariant Identifiers: chr1:g.147380356T>G (hg19) ; chr1:g.147908229T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147908229T>G , CM000663.2:g.147908229T>G	GRCh38
NC_000001.10:g.147380356T>G , CM000663.1:g.147380356T>G	GRCh37
NC_000001.9:g.145846980T>G	NCBI36
NG_016242.1:g.10411T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369235.2:c.274T>G MANE Select	ENSP00000358238.1:p.Tyr92Asp
ENST00000369235.1:c.274T>G	ENSP00000358238.1:p.Tyr92Asp
NM_005267.4:c.274T>G	NP_005258.2:p.Tyr92Asp
XM_011509416.1:c.274T>G	XP_011507718.1:p.Tyr92Asp
XM_011509417.1:c.274T>G	XP_011507719.1:p.Tyr92Asp
XM_011509417.2:c.274T>G	XP_011507719.1:p.Tyr92Asp
XR_002956281.1:n.1189T>G
NM_005267.5:c.274T>G MANE Select	NP_005258.2:p.Tyr92Asp