Canonical Allele Identifier: CA1991957240

Gene: DEUP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93433565T>C , CM000673.2:g.93433565T>C	GRCh38
NC_000011.9:g.93166731T>C , CM000673.1:g.93166731T>C	GRCh37
NC_000011.8:g.92806379T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298050.9:c.1639-3978T>C MANE Select	ENSP00000298050.3:n.1639-3978T>C
ENST00000298050.7:c.1639-3978T>C	ENSP00000298050.3:n.1639-3978T>C
ENST00000525646.1:c.865-3978T>C	ENSP00000435079.1:n.865-3978T>C
ENST00000529909.1:n.280-3978T>C
ENST00000531448.5:c.*110-3978T>C	ENSP00000435527.1:n.*110-3978T>C
ENST00000534747.5:c.*509-3937T>C	ENSP00000432111.2:n.*509-3937T>C
ENST00000618031.4:c.1639-3978T>C	ENSP00000479457.1:n.1639-3978T>C
NM_181645.3:c.1639-3978T>C	NP_857596.2:n.1639-3978T>C
XM_005273802.1:c.1639-3978T>C	XP_005273859.1:n.1639-3978T>C
XM_011542629.1:c.1708-3978T>C	XP_011540931.1:n.1708-3978T>C
XM_011542630.1:c.1708-3978T>C	XP_011540932.1:n.1708-3978T>C
XM_011542631.1:c.1708-3978T>C	XP_011540933.1:n.1708-3978T>C
XM_011542633.1:c.1488-3978T>C	XP_011540935.1:n.1488-3978T>C
XM_011542635.1:c.1327-3978T>C	XP_011540937.1:n.1327-3978T>C
XM_011542636.1:c.934-3978T>C	XP_011540938.1:n.934-3978T>C
XM_011542638.1:c.865-3978T>C	XP_011540940.1:n.865-3978T>C
XR_947796.1:n.1849-1229T>C
XR_947797.1:n.1941-3978T>C
XR_947798.1:n.2175-3978T>C
XR_947799.1:n.2083-3978T>C
XR_947800.1:n.1872-3978T>C
XM_011542629.2:c.1708-3978T>C	XP_011540931.1:n.1708-3978T>C
XM_011542631.2:c.1708-3978T>C	XP_011540933.1:n.1708-3978T>C
XM_011542633.2:c.1488-3978T>C	XP_011540935.1:n.1488-3978T>C
XM_011542635.2:c.1327-3978T>C	XP_011540937.1:n.1327-3978T>C
XM_011542636.2:c.934-3978T>C	XP_011540938.1:n.934-3978T>C
XM_011542638.2:c.865-3978T>C	XP_011540940.1:n.865-3978T>C
XM_017017245.1:c.1708-1229T>C	XP_016872734.1:n.1708-1229T>C
XR_947797.2:n.1930-3978T>C
XR_947798.2:n.2164-3978T>C
XR_947799.2:n.2072-3978T>C
XR_947800.2:n.1861-3978T>C
NM_181645.4:c.1639-3978T>C MANE Select	NP_857596.2:n.1639-3978T>C