Canonical Allele Identifier: CA1917049479

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811584T= , CM000672.2:g.67811584T=	GRCh38
NC_000010.10:g.69571342T= , CM000672.1:g.69571342T=	GRCh37
NC_000010.9:g.69241348T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.237A= MANE Select	ENSP00000225171.2:p.Arg79=
ENST00000225171.6:c.237A=	ENSP00000225171.2:p.Arg79=
ENST00000339758.7:c.237A=	ENSP00000343575.6:p.Arg79=
ENST00000480180.1:c.*256A=	ENSP00000474804.1:n.*256A=
ENST00000480963.5:c.*157A=	ENSP00000473979.1:n.*157A=
ENST00000483798.6:c.327A=	ENSP00000474215.1:p.Arg109=
NM_021800.2:c.237A=	NP_068572.1:p.Arg79=
NM_201262.1:c.237A=	NP_957714.1:p.Arg79=
XM_011539967.1:c.267A=	XP_011538269.1:p.Arg89=
XM_017016431.1:c.-10A=	XP_016871920.1:n.-10A=
XM_017016432.2:c.-10A=	XP_016871921.1:n.-10A=
NM_021800.3:c.237A= MANE Select	NP_068572.1:p.Arg79=
NM_201262.2:c.237A=	NP_957714.1:p.Arg79=