Canonical Allele Identifier: CA1917049457

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811540T= , CM000672.2:g.67811540T=	GRCh38
NC_000010.10:g.69571298T= , CM000672.1:g.69571298T=	GRCh37
NC_000010.9:g.69241304T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.281A= MANE Select	ENSP00000225171.2:p.Asn94=
ENST00000225171.6:c.281A=	ENSP00000225171.2:p.Asn94=
ENST00000339758.7:c.281A=	ENSP00000343575.6:p.Asn94=
ENST00000480180.1:c.*300A=	ENSP00000474804.1:n.*300A=
ENST00000480963.5:c.*201A=	ENSP00000473979.1:n.*201A=
ENST00000483798.6:c.371A=	ENSP00000474215.1:p.Asn124=
NM_021800.2:c.281A=	NP_068572.1:p.Asn94=
NM_201262.1:c.281A=	NP_957714.1:p.Asn94=
XM_011539967.1:c.311A=	XP_011538269.1:p.Asn104=
XM_017016431.1:c.35A=	XP_016871920.1:p.Asn12=
XM_017016432.2:c.35A=	XP_016871921.1:p.Asn12=
NM_021800.3:c.281A= MANE Select	NP_068572.1:p.Asn94=
NM_201262.2:c.281A=	NP_957714.1:p.Asn94=