Canonical Allele Identifier: CA1917049546
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811720C= , CM000672.2:g.67811720C= GRCh38
NC_000010.10:g.69571478C= , CM000672.1:g.69571478C= GRCh37
NC_000010.9:g.69241484C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.158-57G= MANE Select ENSP00000225171.2:n.158-57G=
ENST00000225171.6:c.158-57G= ENSP00000225171.2:n.158-57G=
ENST00000339758.7:c.158-57G= ENSP00000343575.6:n.158-57G=
ENST00000480180.1:c.*177-57G= ENSP00000474804.1:n.*177-57G=
ENST00000480963.5:c.*78-57G= ENSP00000473979.1:n.*78-57G=
ENST00000483798.6:c.248-57G= ENSP00000474215.1:n.248-57G=
NM_021800.2:c.158-57G= NP_068572.1:n.158-57G=
NM_201262.1:c.158-57G= NP_957714.1:n.158-57G=
XM_011539967.1:c.188-57G= XP_011538269.1:n.188-57G=
XM_017016431.1:c.-89-57G= XP_016871920.1:n.-89-57G=
XM_017016432.2:c.-89-57G= XP_016871921.1:n.-89-57G=
NM_021800.3:c.158-57G= MANE Select NP_068572.1:n.158-57G=
NM_201262.2:c.158-57G= NP_957714.1:n.158-57G=