Canonical Allele Identifier: CA169899230

Gene: DNAJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157409969C>G , CM000669.2:g.157409969C>G	GRCh38
NC_000007.13:g.157202663C>G , CM000669.1:g.157202663C>G	GRCh37
NC_000007.12:g.156895424C>G	NCBI36
NG_032573.1:g.77954C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058246.4:c.866C>G MANE Select	NP_490647.1:p.Pro289Arg
ENST00000262177.9:c.866C>G MANE Select	ENSP00000262177.4:p.Pro289Arg
NM_001363676.1:c.521C>G	NP_001350605.1:p.Pro174Arg
NM_058246.3:c.866C>G	NP_490647.1:p.Pro289Arg
ENST00000262177.8:c.866C>G	ENSP00000262177.4:p.Pro289Arg
ENST00000443280.5:c.521C>G	ENSP00000396267.1:p.Pro174Arg
ENST00000459889.5:c.866C>G	ENSP00000488263.1:p.Pro289Arg
ENST00000465908.5:n.662C>G
ENST00000634080.1:c.866C>G	ENSP00000488740.1:p.Pro289Arg
XM_005249515.2:c.866C>G	XP_005249572.1:p.Pro289Arg
XM_005249515.3:c.866C>G	XP_005249572.1:p.Pro289Arg
XM_005249516.2:c.866C>G	XP_005249573.1:p.Pro289Arg
XM_006715823.1:c.692-6047C>G	XP_006715886.1:n.692-6047C>G
XM_006715823.2:c.692-6047C>G	XP_006715886.1:n.692-6047C>G
XM_011515704.1:c.866C>G	XP_011514006.1:p.Pro289Arg