Canonical Allele Identifier: CA377098698
Gene: DNAJC12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811598A>T , CM000672.2:g.67811598A>T GRCh38
NC_000010.10:g.69571356A>T , CM000672.1:g.69571356A>T GRCh37
NC_000010.9:g.69241362A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.223T>A MANE Select ENSP00000225171.2:p.Tyr75Asn
ENST00000225171.6:c.223T>A ENSP00000225171.2:p.Tyr75Asn
ENST00000339758.7:c.223T>A ENSP00000343575.6:p.Tyr75Asn
ENST00000480180.1:c.*242T>A ENSP00000474804.1:n.*242T>A
ENST00000480963.5:c.*143T>A ENSP00000473979.1:n.*143T>A
ENST00000483798.6:c.313T>A ENSP00000474215.1:p.Tyr105Asn
NM_021800.2:c.223T>A NP_068572.1:p.Tyr75Asn
NM_201262.1:c.223T>A NP_957714.1:p.Tyr75Asn
XM_011539967.1:c.253T>A XP_011538269.1:p.Tyr85Asn
XM_017016431.1:c.-24T>A XP_016871920.1:n.-24T>A
XM_017016432.2:c.-24T>A XP_016871921.1:n.-24T>A
NM_021800.3:c.223T>A MANE Select NP_068572.1:p.Tyr75Asn
NM_201262.2:c.223T>A NP_957714.1:p.Tyr75Asn