Canonical Allele Identifier: CA1917049451

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811526T= , CM000672.2:g.67811526T=	GRCh38
NC_000010.10:g.69571284T= , CM000672.1:g.69571284T=	GRCh37
NC_000010.9:g.69241290T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.295A= MANE Select	ENSP00000225171.2:p.Thr99=
ENST00000225171.6:c.295A=	ENSP00000225171.2:p.Thr99=
ENST00000339758.7:c.295A=	ENSP00000343575.6:p.Thr99=
ENST00000480963.5:c.*215A=	ENSP00000473979.1:n.*215A=
ENST00000483798.6:c.385A=	ENSP00000474215.1:p.Thr129=
NM_021800.2:c.295A=	NP_068572.1:p.Thr99=
NM_201262.1:c.295A=	NP_957714.1:p.Thr99=
XM_011539967.1:c.325A=	XP_011538269.1:p.Thr109=
XM_017016431.1:c.49A=	XP_016871920.1:p.Thr17=
XM_017016432.2:c.49A=	XP_016871921.1:p.Thr17=
NM_021800.3:c.295A= MANE Select	NP_068572.1:p.Thr99=
NM_201262.2:c.295A=	NP_957714.1:p.Thr99=