Canonical Allele Identifier: CA1917049472
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811570G= , CM000672.2:g.67811570G= GRCh38
NC_000010.10:g.69571328G= , CM000672.1:g.69571328G= GRCh37
NC_000010.9:g.69241334G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.251C= MANE Select ENSP00000225171.2:p.Ser84=
ENST00000225171.6:c.251C= ENSP00000225171.2:p.Ser84=
ENST00000339758.7:c.251C= ENSP00000343575.6:p.Ser84=
ENST00000480180.1:c.*270C= ENSP00000474804.1:n.*270C=
ENST00000480963.5:c.*171C= ENSP00000473979.1:n.*171C=
ENST00000483798.6:c.341C= ENSP00000474215.1:p.Ser114=
NM_021800.2:c.251C= NP_068572.1:p.Ser84=
NM_201262.1:c.251C= NP_957714.1:p.Ser84=
XM_011539967.1:c.281C= XP_011538269.1:p.Ser94=
XM_017016431.1:c.5C= XP_016871920.1:p.Ser2=
XM_017016432.2:c.5C= XP_016871921.1:p.Ser2=
NM_021800.3:c.251C= MANE Select NP_068572.1:p.Ser84=
NM_201262.2:c.251C= NP_957714.1:p.Ser84=