Canonical Allele Identifier: CA1917049482

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811587C= , CM000672.2:g.67811587C=	GRCh38
NC_000010.10:g.69571345C= , CM000672.1:g.69571345C=	GRCh37
NC_000010.9:g.69241351C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.234G= MANE Select	ENSP00000225171.2:p.Trp78=
ENST00000225171.6:c.234G=	ENSP00000225171.2:p.Trp78=
ENST00000339758.7:c.234G=	ENSP00000343575.6:p.Trp78=
ENST00000480180.1:c.*253G=	ENSP00000474804.1:n.*253G=
ENST00000480963.5:c.*154G=	ENSP00000473979.1:n.*154G=
ENST00000483798.6:c.324G=	ENSP00000474215.1:p.Trp108=
NM_021800.2:c.234G=	NP_068572.1:p.Trp78=
NM_201262.1:c.234G=	NP_957714.1:p.Trp78=
XM_011539967.1:c.264G=	XP_011538269.1:p.Trp88=
XM_017016431.1:c.-13G=	XP_016871920.1:n.-13G=
XM_017016432.2:c.-13G=	XP_016871921.1:n.-13G=
NM_021800.3:c.234G= MANE Select	NP_068572.1:p.Trp78=
NM_201262.2:c.234G=	NP_957714.1:p.Trp78=