Canonical Allele Identifier: CA1917049507
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811628T= , CM000672.2:g.67811628T= GRCh38
NC_000010.10:g.69571386T= , CM000672.1:g.69571386T= GRCh37
NC_000010.9:g.69241392T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.193A= MANE Select ENSP00000225171.2:p.Ile65=
ENST00000225171.6:c.193A= ENSP00000225171.2:p.Ile65=
ENST00000339758.7:c.193A= ENSP00000343575.6:p.Ile65=
ENST00000480180.1:c.*212A= ENSP00000474804.1:n.*212A=
ENST00000480963.5:c.*113A= ENSP00000473979.1:n.*113A=
ENST00000483798.6:c.283A= ENSP00000474215.1:p.Ile95=
NM_021800.2:c.193A= NP_068572.1:p.Ile65=
NM_201262.1:c.193A= NP_957714.1:p.Ile65=
XM_011539967.1:c.223A= XP_011538269.1:p.Ile75=
XM_017016431.1:c.-54A= XP_016871920.1:n.-54A=
XM_017016432.2:c.-54A= XP_016871921.1:n.-54A=
NM_021800.3:c.193A= MANE Select NP_068572.1:p.Ile65=
NM_201262.2:c.193A= NP_957714.1:p.Ile65=