Canonical Allele Identifier: CA370166628

Gene: DNAJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157384887C>G , CM000669.2:g.157384887C>G	GRCh38
NC_000007.13:g.157177581C>G , CM000669.1:g.157177581C>G	GRCh37
NC_000007.12:g.156870342C>G	NCBI36
NG_032573.1:g.52872C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.499C>G MANE Select	ENSP00000262177.4:p.Leu167Val
ENST00000262177.8:c.499C>G	ENSP00000262177.4:p.Leu167Val
ENST00000417758.5:c.499C>G	ENSP00000400665.1:p.Leu167Val
ENST00000429029.6:c.499C>G	ENSP00000397556.2:p.Leu167Val
ENST00000443280.5:c.346+17404C>G	ENSP00000396267.1:n.346+17404C>G
ENST00000459889.5:c.499C>G	ENSP00000488263.1:p.Leu167Val
ENST00000465908.5:n.295C>G
ENST00000468928.5:n.804C>G
ENST00000487480.1:n.4274C>G
ENST00000634080.1:c.499C>G	ENSP00000488740.1:p.Leu167Val
NM_005494.2:c.499C>G	NP_005485.1:p.Leu167Val
NM_058246.3:c.499C>G	NP_490647.1:p.Leu167Val
XM_005249515.2:c.499C>G	XP_005249572.1:p.Leu167Val
XM_005249516.2:c.499C>G	XP_005249573.1:p.Leu167Val
XM_006715823.1:c.499C>G	XP_006715886.1:p.Leu167Val
XM_011515704.1:c.499C>G	XP_011514006.1:p.Leu167Val
NM_001363676.1:c.346+17404C>G	NP_001350605.1:n.346+17404C>G
XM_005249515.3:c.499C>G	XP_005249572.1:p.Leu167Val
XM_006715823.2:c.499C>G	XP_006715886.1:p.Leu167Val
NM_058246.4:c.499C>G MANE Select	NP_490647.1:p.Leu167Val
NM_005494.3:c.499C>G	NP_005485.1:p.Leu167Val