Canonical Allele Identifier: CA1917049398

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811416T= , CM000672.2:g.67811416T=	GRCh38
NC_000010.10:g.69571174T= , CM000672.1:g.69571174T=	GRCh37
NC_000010.9:g.69241180T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.297+108A= MANE Select	ENSP00000225171.2:n.297+108A=
ENST00000225171.6:c.297+108A=	ENSP00000225171.2:n.297+108A=
ENST00000339758.7:c.*81A=	ENSP00000343575.6:n.*81A=
ENST00000480963.5:c.*217+108A=	ENSP00000473979.1:n.*217+108A=
ENST00000483798.6:c.387+108A=	ENSP00000474215.1:n.387+108A=
NM_021800.2:c.297+108A=	NP_068572.1:n.297+108A=
NM_201262.1:c.*81A=	NP_957714.1:n.*81A=
XM_011539967.1:c.327+108A=	XP_011538269.1:n.327+108A=
XM_017016431.1:c.51+108A=	XP_016871920.1:n.51+108A=
XM_017016432.2:c.51+108A=	XP_016871921.1:n.51+108A=
NM_021800.3:c.297+108A= MANE Select	NP_068572.1:n.297+108A=
NM_201262.2:c.*81A=	NP_957714.1:n.*81A=