Canonical Allele Identifier: CA83594745

Gene: DNAJC13

Linked Data

• dbSNP Id: rs1378810
• MyVariant Identifiers: chr3:g.132535246A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132535246A>C , CM000665.2:g.132535246A>C	GRCh38
NC_000003.11:g.132254090A>C , CM000665.1:g.132254090A>C	GRCh37
NC_000003.10:g.133736780A>C	NCBI36
NG_051045.1:g.122720A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260818.11:c.6626-2930A>C MANE Select	ENSP00000260818.6:n.6626-2930A>C
ENST00000650455.1:c.*4900-2930A>C	ENSP00000496825.1:n.*4900-2930A>C
ENST00000260818.10:c.6626-2930A>C	ENSP00000260818.6:n.6626-2930A>C
ENST00000509279.1:c.232-1912A>C
NM_015268.3:c.6626-2930A>C	NP_056083.3:n.6626-2930A>C
XM_005247245.3:c.6641-2930A>C	XP_005247302.1:n.6641-2930A>C
NM_001329126.1:c.6641-2930A>C	NP_001316055.1:n.6641-2930A>C
XM_017006036.1:c.4595-2930A>C	XP_016861525.1:n.4595-2930A>C
NM_015268.4:c.6626-2930A>C MANE Select	NP_056083.3:n.6626-2930A>C
NM_001329126.2:c.6641-2930A>C	NP_001316055.1:n.6641-2930A>C