Canonical Allele Identifier: CA458781448

Gene: DNAJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157409904G>A , CM000669.2:g.157409904G>A	GRCh38
NC_000007.13:g.157202598G>A , CM000669.1:g.157202598G>A	GRCh37
NC_000007.12:g.156895359G>A	NCBI36
NG_032573.1:g.77889G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058246.4:c.801G>A MANE Select	NP_490647.1:p.Ser267=
ENST00000262177.9:c.801G>A MANE Select	ENSP00000262177.4:p.Ser267=
NM_001363676.1:c.456G>A	NP_001350605.1:p.Ser152=
NM_058246.3:c.801G>A	NP_490647.1:p.Ser267=
ENST00000262177.8:c.801G>A	ENSP00000262177.4:p.Ser267=
ENST00000443280.5:c.456G>A	ENSP00000396267.1:p.Ser152=
ENST00000459889.5:c.801G>A	ENSP00000488263.1:p.Ser267=
ENST00000465908.5:n.597G>A
ENST00000634080.1:c.801G>A	ENSP00000488740.1:p.Ser267=
XM_005249515.2:c.801G>A	XP_005249572.1:p.Ser267=
XM_005249515.3:c.801G>A	XP_005249572.1:p.Ser267=
XM_005249516.2:c.801G>A	XP_005249573.1:p.Ser267=
XM_006715823.1:c.692-6112G>A	XP_006715886.1:n.692-6112G>A
XM_006715823.2:c.692-6112G>A	XP_006715886.1:n.692-6112G>A
XM_011515704.1:c.801G>A	XP_011514006.1:p.Ser267=