Canonical Allele Identifier: CA1917049466

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811561A= , CM000672.2:g.67811561A=	GRCh38
NC_000010.10:g.69571319A= , CM000672.1:g.69571319A=	GRCh37
NC_000010.9:g.69241325A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.260T= MANE Select	ENSP00000225171.2:p.Phe87=
ENST00000225171.6:c.260T=	ENSP00000225171.2:p.Phe87=
ENST00000339758.7:c.260T=	ENSP00000343575.6:p.Phe87=
ENST00000480180.1:c.*279T=	ENSP00000474804.1:n.*279T=
ENST00000480963.5:c.*180T=	ENSP00000473979.1:n.*180T=
ENST00000483798.6:c.350T=	ENSP00000474215.1:p.Phe117=
NM_021800.2:c.260T=	NP_068572.1:p.Phe87=
NM_201262.1:c.260T=	NP_957714.1:p.Phe87=
XM_011539967.1:c.290T=	XP_011538269.1:p.Phe97=
XM_017016431.1:c.14T=	XP_016871920.1:p.Phe5=
XM_017016432.2:c.14T=	XP_016871921.1:p.Phe5=
NM_021800.3:c.260T= MANE Select	NP_068572.1:p.Phe87=
NM_201262.2:c.260T=	NP_957714.1:p.Phe87=