Canonical Allele Identifier: CA1917049442
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811512C= , CM000672.2:g.67811512C= GRCh38
NC_000010.10:g.69571270C= , CM000672.1:g.69571270C= GRCh37
NC_000010.9:g.69241276C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000225171.7:c.297+12G= MANE Select ENSP00000225171.2:n.297+12G=
ENST00000225171.6:c.297+12G= ENSP00000225171.2:n.297+12G=
ENST00000339758.7:c.309G= ENSP00000343575.6:p.Ser103=
ENST00000480963.5:c.*217+12G= ENSP00000473979.1:n.*217+12G=
ENST00000483798.6:c.387+12G= ENSP00000474215.1:n.387+12G=
NM_021800.2:c.297+12G= NP_068572.1:n.297+12G=
NM_201262.1:c.309G= NP_957714.1:p.Ser103=
XM_011539967.1:c.327+12G= XP_011538269.1:n.327+12G=
XM_017016431.1:c.51+12G= XP_016871920.1:n.51+12G=
XM_017016432.2:c.51+12G= XP_016871921.1:n.51+12G=
NM_021800.3:c.297+12G= MANE Select NP_068572.1:n.297+12G=
NM_201262.2:c.309G= NP_957714.1:p.Ser103=