Canonical Allele Identifier: CA1917049508
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811632C= , CM000672.2:g.67811632C= GRCh38
NC_000010.10:g.69571390C= , CM000672.1:g.69571390C= GRCh37
NC_000010.9:g.69241396C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000225171.7:c.189G= MANE Select ENSP00000225171.2:p.Lys63=
ENST00000225171.6:c.189G= ENSP00000225171.2:p.Lys63=
ENST00000339758.7:c.189G= ENSP00000343575.6:p.Lys63=
ENST00000480180.1:c.*208G= ENSP00000474804.1:n.*208G=
ENST00000480963.5:c.*109G= ENSP00000473979.1:n.*109G=
ENST00000483798.6:c.279G= ENSP00000474215.1:p.Lys93=
NM_021800.2:c.189G= NP_068572.1:p.Lys63=
NM_201262.1:c.189G= NP_957714.1:p.Lys63=
XM_011539967.1:c.219G= XP_011538269.1:p.Lys73=
XM_017016431.1:c.-58G= XP_016871920.1:n.-58G=
XM_017016432.2:c.-58G= XP_016871921.1:n.-58G=
NM_021800.3:c.189G= MANE Select NP_068572.1:p.Lys63=
NM_201262.2:c.189G= NP_957714.1:p.Lys63=