Canonical Allele Identifier: CA1917049443
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811513G= , CM000672.2:g.67811513G= GRCh38
NC_000010.10:g.69571271G= , CM000672.1:g.69571271G= GRCh37
NC_000010.9:g.69241277G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000225171.7:c.297+11C= MANE Select ENSP00000225171.2:n.297+11C=
ENST00000225171.6:c.297+11C= ENSP00000225171.2:n.297+11C=
ENST00000339758.7:c.308C= ENSP00000343575.6:p.Ser103=
ENST00000480963.5:c.*217+11C= ENSP00000473979.1:n.*217+11C=
ENST00000483798.6:c.387+11C= ENSP00000474215.1:n.387+11C=
NM_021800.2:c.297+11C= NP_068572.1:n.297+11C=
NM_201262.1:c.308C= NP_957714.1:p.Ser103=
XM_011539967.1:c.327+11C= XP_011538269.1:n.327+11C=
XM_017016431.1:c.51+11C= XP_016871920.1:n.51+11C=
XM_017016432.2:c.51+11C= XP_016871921.1:n.51+11C=
NM_021800.3:c.297+11C= MANE Select NP_068572.1:n.297+11C=
NM_201262.2:c.308C= NP_957714.1:p.Ser103=