Canonical Allele Identifier: CA1917049499

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811610T= , CM000672.2:g.67811610T=	GRCh38
NC_000010.10:g.69571368T= , CM000672.1:g.69571368T=	GRCh37
NC_000010.9:g.69241374T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.211A= MANE Select	ENSP00000225171.2:p.Ser71=
ENST00000225171.6:c.211A=	ENSP00000225171.2:p.Ser71=
ENST00000339758.7:c.211A=	ENSP00000343575.6:p.Ser71=
ENST00000480180.1:c.*230A=	ENSP00000474804.1:n.*230A=
ENST00000480963.5:c.*131A=	ENSP00000473979.1:n.*131A=
ENST00000483798.6:c.301A=	ENSP00000474215.1:p.Ser101=
NM_021800.2:c.211A=	NP_068572.1:p.Ser71=
NM_201262.1:c.211A=	NP_957714.1:p.Ser71=
XM_011539967.1:c.241A=	XP_011538269.1:p.Ser81=
XM_017016431.1:c.-36A=	XP_016871920.1:n.-36A=
XM_017016432.2:c.-36A=	XP_016871921.1:n.-36A=
NM_021800.3:c.211A= MANE Select	NP_068572.1:p.Ser71=
NM_201262.2:c.211A=	NP_957714.1:p.Ser71=