Canonical Allele Identifier: CA10586324

Gene: DNAJB13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73951138G>C , CM000673.2:g.73951138G>C	GRCh38
NC_000011.9:g.73662183G>C , CM000673.1:g.73662183G>C	GRCh37
NC_000011.8:g.73339831G>C	NCBI36
NG_053111.1:g.5820G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339764.6:c.68+1G>C MANE Select	ENSP00000344431.1:n.68+1G>C
ENST00000339764.5:c.68+1G>C	ENSP00000344431.1:n.68+1G>C
ENST00000535730.1:n.112+1G>C
NM_153614.3:c.68+1G>C	NP_705842.2:n.68+1G>C
XM_005273984.2:c.68+1G>C	XP_005274041.1:n.68+1G>C
XM_011545004.1:c.-390+1G>C	XP_011543306.1:n.-390+1G>C
XM_011545005.1:c.-390+1G>C	XP_011543307.1:n.-390+1G>C
XM_011545006.1:c.-376+1G>C	XP_011543308.1:n.-376+1G>C
XM_011545008.1:c.-700+1G>C	XP_011543310.1:n.-700+1G>C
XM_011545009.1:c.-507+1G>C	XP_011543311.1:n.-507+1G>C
XM_011545010.1:c.-704+1G>C	XP_011543312.1:n.-704+1G>C
XM_011545011.1:c.-569+1G>C	XP_011543313.1:n.-569+1G>C
XM_011545012.1:c.-380+1G>C	XP_011543314.1:n.-380+1G>C
XM_011545013.1:c.-390+1G>C	XP_011543315.1:n.-390+1G>C
XM_011545014.1:c.-390+1G>C	XP_011543316.1:n.-390+1G>C
XR_949909.1:n.89+1G>C
XM_005273984.3:c.68+1G>C	XP_005274041.1:n.68+1G>C
XM_011545004.3:c.-390+1G>C	XP_011543306.1:n.-390+1G>C
XM_011545005.2:c.-390+1G>C	XP_011543307.1:n.-390+1G>C
XM_011545009.3:c.-507+1G>C	XP_011543311.1:n.-507+1G>C
XM_011545013.2:c.-390+1G>C	XP_011543315.1:n.-390+1G>C
XM_011545014.2:c.-390+1G>C	XP_011543316.1:n.-390+1G>C
XM_017017679.1:c.-390+1G>C	XP_016873168.1:n.-390+1G>C
XM_024448506.1:c.-238+1G>C	XP_024304274.1:n.-238+1G>C
XM_024448507.1:c.-376+1G>C	XP_024304275.1:n.-376+1G>C
XM_024448508.1:c.-700+1G>C	XP_024304276.1:n.-700+1G>C
XM_024448509.1:c.-569+1G>C	XP_024304277.1:n.-569+1G>C
XM_024448510.1:c.-380+1G>C	XP_024304278.1:n.-380+1G>C
XR_949909.2:n.517+1G>C
NM_001377263.1:c.-238+1G>C	NP_001364192.1:n.-238+1G>C
NM_153614.4:c.68+1G>C MANE Select	NP_705842.2:n.68+1G>C