Canonical Allele Identifier: CA1917049408

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811443A= , CM000672.2:g.67811443A=	GRCh38
NC_000010.10:g.69571201A= , CM000672.1:g.69571201A=	GRCh37
NC_000010.9:g.69241207A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.297+81T= MANE Select	ENSP00000225171.2:n.297+81T=
ENST00000225171.6:c.297+81T=	ENSP00000225171.2:n.297+81T=
ENST00000339758.7:c.*54T=	ENSP00000343575.6:n.*54T=
ENST00000480963.5:c.*217+81T=	ENSP00000473979.1:n.*217+81T=
ENST00000483798.6:c.387+81T=	ENSP00000474215.1:n.387+81T=
NM_021800.2:c.297+81T=	NP_068572.1:n.297+81T=
NM_201262.1:c.*54T=	NP_957714.1:n.*54T=
XM_011539967.1:c.327+81T=	XP_011538269.1:n.327+81T=
XM_017016431.1:c.51+81T=	XP_016871920.1:n.51+81T=
XM_017016432.2:c.51+81T=	XP_016871921.1:n.51+81T=
NM_021800.3:c.297+81T= MANE Select	NP_068572.1:n.297+81T=
NM_201262.2:c.*54T=	NP_957714.1:n.*54T=