Canonical Allele Identifier: CA9969744
Community Standard Title: NM_025219.3(DNAJC5):c.429C>T (p.Gly143=)
Gene: DNAJC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63930958C>T , CM000682.2:g.63930958C>T GRCh38
NC_000020.10:g.62562311C>T , CM000682.1:g.62562311C>T GRCh37
NC_000020.9:g.62032755C>T NCBI36
NG_029805.1:g.40857C>T
NG_029805.2:g.40857C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025219.3:c.429C>T MANE Select NP_079495.1:p.Gly143=
ENST00000360864.9:c.429C>T MANE Select ENSP00000354111.4:p.Gly143=
NM_025219.2:c.429C>T NP_079495.1:p.Gly143=
ENST00000360864.8:c.429C>T ENSP00000354111.4:p.Gly143=
ENST00000470551.1:c.429C>T ENSP00000434744.1:p.Gly143=
ENST00000703637.1:c.429C>T ENSP00000515413.1:p.Gly143=
XM_011529048.1:c.429C>T XP_011527350.1:p.Gly143=
XM_011529048.2:c.429C>T XP_011527350.1:p.Gly143=
XM_011529049.1:c.429C>T XP_011527351.1:p.Gly143=
XM_011529050.1:c.429C>T XP_011527352.1:p.Gly143=
XR_936629.1:n.1061C>T
XR_936629.2:n.1074C>T
XR_936630.1:n.1319C>T