Canonical Allele Identifier: CA209166004
Gene: DNAJC12 HGNC NCBI

Linked Data

dbSNP Id: rs200885499

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811540T>C , CM000672.2:g.67811540T>C GRCh38
NC_000010.10:g.69571298T>C , CM000672.1:g.69571298T>C GRCh37
NC_000010.9:g.69241304T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.281A>G MANE Select ENSP00000225171.2:p.Asn94Ser
ENST00000225171.6:c.281A>G ENSP00000225171.2:p.Asn94Ser
ENST00000339758.7:c.281A>G ENSP00000343575.6:p.Asn94Ser
ENST00000480180.1:c.*300A>G ENSP00000474804.1:n.*300A>G
ENST00000480963.5:c.*201A>G ENSP00000473979.1:n.*201A>G
ENST00000483798.6:c.371A>G ENSP00000474215.1:p.Asn124Ser
NM_021800.2:c.281A>G NP_068572.1:p.Asn94Ser
NM_201262.1:c.281A>G NP_957714.1:p.Asn94Ser
XM_011539967.1:c.311A>G XP_011538269.1:p.Asn104Ser
XM_017016431.1:c.35A>G XP_016871920.1:p.Asn12Ser
XM_017016432.2:c.35A>G XP_016871921.1:p.Asn12Ser
NM_021800.3:c.281A>G MANE Select NP_068572.1:p.Asn94Ser
NM_201262.2:c.281A>G NP_957714.1:p.Asn94Ser