Canonical Allele Identifier: CA370167184

Gene: DNAJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157409818G>C , CM000669.2:g.157409818G>C	GRCh38
NC_000007.13:g.157202512G>C , CM000669.1:g.157202512G>C	GRCh37
NC_000007.12:g.156895273G>C	NCBI36
NG_032573.1:g.77803G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_058246.4:c.715G>C MANE Select	NP_490647.1:p.Ala239Pro
ENST00000262177.9:c.715G>C MANE Select	ENSP00000262177.4:p.Ala239Pro
NM_001363676.1:c.370G>C	NP_001350605.1:p.Ala124Pro
NM_058246.3:c.715G>C	NP_490647.1:p.Ala239Pro
ENST00000262177.8:c.715G>C	ENSP00000262177.4:p.Ala239Pro
ENST00000443280.5:c.370G>C	ENSP00000396267.1:p.Ala124Pro
ENST00000459889.5:c.715G>C	ENSP00000488263.1:p.Ala239Pro
ENST00000465908.5:n.511G>C
ENST00000634080.1:c.715G>C	ENSP00000488740.1:p.Ala239Pro
XM_005249515.2:c.715G>C	XP_005249572.1:p.Ala239Pro
XM_005249515.3:c.715G>C	XP_005249572.1:p.Ala239Pro
XM_005249516.2:c.715G>C	XP_005249573.1:p.Ala239Pro
XM_006715823.1:c.692-6198G>C	XP_006715886.1:n.692-6198G>C
XM_006715823.2:c.692-6198G>C	XP_006715886.1:n.692-6198G>C
XM_011515704.1:c.715G>C	XP_011514006.1:p.Ala239Pro