Canonical Allele Identifier: CA1917049478

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811583T= , CM000672.2:g.67811583T=	GRCh38
NC_000010.10:g.69571341T= , CM000672.1:g.69571341T=	GRCh37
NC_000010.9:g.69241347T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.238A= MANE Select	ENSP00000225171.2:p.Arg80=
ENST00000225171.6:c.238A=	ENSP00000225171.2:p.Arg80=
ENST00000339758.7:c.238A=	ENSP00000343575.6:p.Arg80=
ENST00000480180.1:c.*257A=	ENSP00000474804.1:n.*257A=
ENST00000480963.5:c.*158A=	ENSP00000473979.1:n.*158A=
ENST00000483798.6:c.328A=	ENSP00000474215.1:p.Arg110=
NM_021800.2:c.238A=	NP_068572.1:p.Arg80=
NM_201262.1:c.238A=	NP_957714.1:p.Arg80=
XM_011539967.1:c.268A=	XP_011538269.1:p.Arg90=
XM_017016431.1:c.-9A=	XP_016871920.1:n.-9A=
XM_017016432.2:c.-9A=	XP_016871921.1:n.-9A=
NM_021800.3:c.238A= MANE Select	NP_068572.1:p.Arg80=
NM_201262.2:c.238A=	NP_957714.1:p.Arg80=