Canonical Allele Identifier: CA381807523

Gene: DNAJB13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73966137G>A , CM000673.2:g.73966137G>A	GRCh38
NC_000011.9:g.73677182G>A , CM000673.1:g.73677182G>A	GRCh37
NC_000011.8:g.73354830G>A	NCBI36
NG_053111.1:g.20819G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_153614.4:c.493-1G>A MANE Select	NP_705842.2:n.493-1G>A
ENST00000339764.6:c.493-1G>A MANE Select	ENSP00000344431.1:n.493-1G>A
NM_001377263.1:c.319-1G>A	NP_001364192.1:n.319-1G>A
NM_153614.3:c.493-1G>A	NP_705842.2:n.493-1G>A
ENST00000339764.5:c.493-1G>A	ENSP00000344431.1:n.493-1G>A
ENST00000537753.5:c.-162-1G>A	ENSP00000439711.1:n.-162-1G>A
ENST00000542350.5:c.194-1G>A
ENST00000543947.1:c.-347G>A	ENSP00000438576.1:n.-347G>A
XM_005273984.2:c.331-1G>A	XP_005274041.1:n.331-1G>A
XM_005273984.3:c.331-1G>A	XP_005274041.1:n.331-1G>A
XM_011545004.1:c.595-1G>A	XP_011543306.1:n.595-1G>A
XM_011545004.3:c.595-1G>A	XP_011543306.1:n.595-1G>A
XM_011545005.1:c.433-1G>A	XP_011543307.1:n.433-1G>A
XM_011545005.2:c.433-1G>A	XP_011543307.1:n.433-1G>A
XM_011545006.1:c.319-1G>A	XP_011543308.1:n.319-1G>A
XM_011545007.1:c.319-1G>A	XP_011543309.1:n.319-1G>A
XM_011545007.2:c.319-1G>A	XP_011543309.1:n.319-1G>A
XM_011545008.1:c.319-1G>A	XP_011543310.1:n.319-1G>A
XM_011545009.1:c.319-1G>A	XP_011543311.1:n.319-1G>A
XM_011545009.3:c.319-1G>A	XP_011543311.1:n.319-1G>A
XM_011545010.1:c.319-1G>A	XP_011543312.1:n.319-1G>A
XM_011545011.1:c.319-1G>A	XP_011543313.1:n.319-1G>A
XM_011545012.1:c.319-1G>A	XP_011543314.1:n.319-1G>A
XM_011545013.1:c.595-1G>A	XP_011543315.1:n.595-1G>A
XM_011545013.2:c.595-1G>A	XP_011543315.1:n.595-1G>A
XM_011545015.1:c.70-1G>A	XP_011543317.1:n.70-1G>A
XM_011545015.2:c.70-1G>A	XP_011543317.1:n.70-1G>A
XM_017017675.1:c.319-1G>A	XP_016873164.1:n.319-1G>A
XM_024448506.1:c.319-1G>A	XP_024304274.1:n.319-1G>A
XM_024448507.1:c.319-1G>A	XP_024304275.1:n.319-1G>A
XM_024448508.1:c.319-1G>A	XP_024304276.1:n.319-1G>A
XM_024448509.1:c.319-1G>A	XP_024304277.1:n.319-1G>A
XM_024448510.1:c.319-1G>A	XP_024304278.1:n.319-1G>A
XR_949909.1:n.1073-1G>A
XR_949909.2:n.1501-1G>A