Canonical Allele Identifier: CA6180746

Gene: DNAJB13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73964917T>G , CM000673.2:g.73964917T>G	GRCh38
NC_000011.9:g.73675962T>G , CM000673.1:g.73675962T>G	GRCh37
NC_000011.8:g.73353610T>G	NCBI36
NG_053111.1:g.19599T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_153614.4:c.374T>G MANE Select	NP_705842.2:p.Phe125Cys
ENST00000339764.6:c.374T>G MANE Select	ENSP00000344431.1:p.Phe125Cys
NM_001377263.1:c.200T>G	NP_001364192.1:p.Phe67Cys
NM_153614.3:c.374T>G	NP_705842.2:p.Phe125Cys
ENST00000339764.5:c.374T>G	ENSP00000344431.1:p.Phe125Cys
ENST00000537753.5:c.-281T>G	ENSP00000439711.1:n.-281T>G
ENST00000542350.5:c.75T>G
XM_005273984.2:c.212T>G	XP_005274041.1:p.Phe71Cys
XM_005273984.3:c.212T>G	XP_005274041.1:p.Phe71Cys
XM_011545004.1:c.476T>G	XP_011543306.1:p.Phe159Cys
XM_011545004.3:c.476T>G	XP_011543306.1:p.Phe159Cys
XM_011545005.1:c.314T>G	XP_011543307.1:p.Phe105Cys
XM_011545005.2:c.314T>G	XP_011543307.1:p.Phe105Cys
XM_011545006.1:c.200T>G	XP_011543308.1:p.Phe67Cys
XM_011545007.1:c.200T>G	XP_011543309.1:p.Phe67Cys
XM_011545007.2:c.200T>G	XP_011543309.1:p.Phe67Cys
XM_011545008.1:c.200T>G	XP_011543310.1:p.Phe67Cys
XM_011545009.1:c.200T>G	XP_011543311.1:p.Phe67Cys
XM_011545009.3:c.200T>G	XP_011543311.1:p.Phe67Cys
XM_011545010.1:c.200T>G	XP_011543312.1:p.Phe67Cys
XM_011545011.1:c.200T>G	XP_011543313.1:p.Phe67Cys
XM_011545012.1:c.200T>G	XP_011543314.1:p.Phe67Cys
XM_011545013.1:c.476T>G	XP_011543315.1:p.Phe159Cys
XM_011545013.2:c.476T>G	XP_011543315.1:p.Phe159Cys
XM_011545014.1:c.*48T>G	XP_011543316.1:n.*48T>G
XM_011545014.2:c.*48T>G	XP_011543316.1:n.*48T>G
XM_017017675.1:c.200T>G	XP_016873164.1:p.Phe67Cys
XM_024448506.1:c.200T>G	XP_024304274.1:p.Phe67Cys
XM_024448507.1:c.200T>G	XP_024304275.1:p.Phe67Cys
XM_024448508.1:c.200T>G	XP_024304276.1:p.Phe67Cys
XM_024448509.1:c.200T>G	XP_024304277.1:p.Phe67Cys
XM_024448510.1:c.200T>G	XP_024304278.1:p.Phe67Cys
XR_949909.1:n.954T>G
XR_949909.2:n.1382T>G