Canonical Allele Identifier: CA354566890
Gene: DNAJC13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132477995A>C , CM000665.2:g.132477995A>C GRCh38
NC_000003.11:g.132196839A>C , CM000665.1:g.132196839A>C GRCh37
NC_000003.10:g.133679529A>C NCBI36
NG_051045.1:g.65469A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260818.11:c.2564A>C MANE Select ENSP00000260818.6:p.Asn855Thr
ENST00000650455.1:c.*712A>C ENSP00000496825.1:n.*712A>C
ENST00000260818.10:c.2564A>C ENSP00000260818.6:p.Asn855Thr
ENST00000464766.1:n.401A>C
NM_015268.3:c.2564A>C NP_056083.3:p.Asn855Thr
XM_005247245.3:c.2579A>C XP_005247302.1:p.Asn860Thr
NM_001329126.1:c.2579A>C NP_001316055.1:p.Asn860Thr
XM_017006036.1:c.533A>C XP_016861525.1:p.Asn178Thr
NM_015268.4:c.2564A>C MANE Select NP_056083.3:p.Asn855Thr
NM_001329126.2:c.2579A>C NP_001316055.1:p.Asn860Thr