Canonical Allele Identifier: CA2737103232
Gene: DNAJC5 HGNC NCBI

Linked Data

dbSNP Id: rs2146311804

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63933067_63933068insCC , CM000682.2:g.63933067_63933068insCC GRCh38
NC_000020.10:g.62564420_62564421insCC , CM000682.1:g.62564420_62564421insCC GRCh37
NC_000020.9:g.62034864_62034865insCC NCBI36
NG_029805.1:g.42966_42967insCC
NG_029805.2:g.42966_42967insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000703637.1:c.*1666_*1667insCC ENSP00000515413.1:n.*1666_*1667insCC
ENST00000360864.9:c.*1499_*1500insCC MANE Select ENSP00000354111.4:n.*1499_*1500insCC
ENST00000360864.8:c.*1499_*1500insCC ENSP00000354111.4:n.*1499_*1500insCC
ENST00000470551.1:c.*1666_*1667insCC ENSP00000434744.1:n.*1666_*1667insCC
NM_025219.2:c.*1499_*1500insCC NP_079495.1:n.*1499_*1500insCC
XM_011529048.1:c.*1499_*1500insCC XP_011527350.1:n.*1499_*1500insCC
XM_011529049.1:c.*1499_*1500insCC XP_011527351.1:n.*1499_*1500insCC
XM_011529050.1:c.*1499_*1500insCC XP_011527352.1:n.*1499_*1500insCC
XR_936629.1:n.2802_2803insCC
XR_936630.1:n.3060_3061insCC
XM_011529048.2:c.*1499_*1500insCC XP_011527350.1:n.*1499_*1500insCC
XR_936629.2:n.2815_2816insCC
NM_025219.3:c.*1499_*1500insCC MANE Select NP_079495.1:n.*1499_*1500insCC