Canonical Allele Identifier: CA1917049485
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811593G= , CM000672.2:g.67811593G= GRCh38
NC_000010.10:g.69571351G= , CM000672.1:g.69571351G= GRCh37
NC_000010.9:g.69241357G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.228C= MANE Select ENSP00000225171.2:p.Asp76=
ENST00000225171.6:c.228C= ENSP00000225171.2:p.Asp76=
ENST00000339758.7:c.228C= ENSP00000343575.6:p.Asp76=
ENST00000480180.1:c.*247C= ENSP00000474804.1:n.*247C=
ENST00000480963.5:c.*148C= ENSP00000473979.1:n.*148C=
ENST00000483798.6:c.318C= ENSP00000474215.1:p.Asp106=
NM_021800.2:c.228C= NP_068572.1:p.Asp76=
NM_201262.1:c.228C= NP_957714.1:p.Asp76=
XM_011539967.1:c.258C= XP_011538269.1:p.Asp86=
XM_017016431.1:c.-19C= XP_016871920.1:n.-19C=
XM_017016432.2:c.-19C= XP_016871921.1:n.-19C=
NM_021800.3:c.228C= MANE Select NP_068572.1:p.Asp76=
NM_201262.2:c.228C= NP_957714.1:p.Asp76=