Canonical Allele Identifier: CA377098747
Gene: DNAJC12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811622T>G , CM000672.2:g.67811622T>G GRCh38
NC_000010.10:g.69571380T>G , CM000672.1:g.69571380T>G GRCh37
NC_000010.9:g.69241386T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.199A>C MANE Select ENSP00000225171.2:p.Thr67Pro
ENST00000225171.6:c.199A>C ENSP00000225171.2:p.Thr67Pro
ENST00000339758.7:c.199A>C ENSP00000343575.6:p.Thr67Pro
ENST00000480180.1:c.*218A>C ENSP00000474804.1:n.*218A>C
ENST00000480963.5:c.*119A>C ENSP00000473979.1:n.*119A>C
ENST00000483798.6:c.289A>C ENSP00000474215.1:p.Thr97Pro
NM_021800.2:c.199A>C NP_068572.1:p.Thr67Pro
NM_201262.1:c.199A>C NP_957714.1:p.Thr67Pro
XM_011539967.1:c.229A>C XP_011538269.1:p.Thr77Pro
XM_017016431.1:c.-48A>C XP_016871920.1:n.-48A>C
XM_017016432.2:c.-48A>C XP_016871921.1:n.-48A>C
NM_021800.3:c.199A>C MANE Select NP_068572.1:p.Thr67Pro
NM_201262.2:c.199A>C NP_957714.1:p.Thr67Pro