Canonical Allele Identifier: CA365535051

Gene: DSE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116399667G>A , CM000668.2:g.116399667G>A	GRCh38
NC_000006.11:g.116720830G>A , CM000668.1:g.116720830G>A	GRCh37
NC_000006.10:g.116827523G>A	NCBI36
NG_033266.1:g.124548G>A
NG_033266.3:g.150516G>A
NG_033266.4:g.150497G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_013352.4:c.416+1G>A MANE Select	NP_037484.1:n.416+1G>A
ENST00000644252.3:c.416+1G>A MANE Select	ENSP00000494147.2:n.416+1G>A
NM_001080976.1:c.416+1G>A	NP_001074445.1:n.416+1G>A
NM_001080976.2:c.416+1G>A	NP_001074445.1:n.416+1G>A
NM_001080976.3:c.416+1G>A	NP_001074445.1:n.416+1G>A
NM_001322937.1:c.416+1G>A	NP_001309866.1:n.416+1G>A
NM_001322937.2:c.416+1G>A	NP_001309866.1:n.416+1G>A
NM_001322938.1:c.416+1G>A	NP_001309867.1:n.416+1G>A
NM_001322938.2:c.416+1G>A	NP_001309867.1:n.416+1G>A
NM_001322939.1:c.473+1G>A	NP_001309868.1:n.473+1G>A
NM_001322939.2:c.473+1G>A	NP_001309868.1:n.473+1G>A
NM_001322940.1:c.-146+5G>A	NP_001309869.1:n.-146+5G>A
NM_001322940.2:c.-146+5G>A	NP_001309869.1:n.-146+5G>A
NM_001322941.1:c.-146+5G>A	NP_001309870.1:n.-146+5G>A
NM_001322941.2:c.-146+5G>A	NP_001309870.1:n.-146+5G>A
NM_001322943.1:c.416+1G>A	NP_001309872.1:n.416+1G>A
NM_001322943.2:c.416+1G>A	NP_001309872.1:n.416+1G>A
NM_001322944.1:c.416+1G>A	NP_001309873.1:n.416+1G>A
NM_001322944.2:c.416+1G>A	NP_001309873.1:n.416+1G>A
NM_001374520.1:c.-485+1G>A	NP_001361449.1:n.-485+1G>A
NM_001374521.1:c.-172+1G>A	NP_001361450.1:n.-172+1G>A
NM_001374522.1:c.416+1G>A	NP_001361451.1:n.416+1G>A
NM_013352.2:c.416+1G>A	NP_037484.1:n.416+1G>A
NM_013352.3:c.416+1G>A	NP_037484.1:n.416+1G>A
NR_136524.1:n.663+5G>A
NR_136524.2:n.640+5G>A
ENST00000331677.7:c.416+1G>A	ENSP00000332151.2:n.416+1G>A
ENST00000359564.2:c.416+1G>A	ENSP00000352567.2:n.416+1G>A
ENST00000359564.3:c.416+1G>A	ENSP00000352567.3:n.416+1G>A
ENST00000430252.6:c.416+1G>A	ENSP00000397597.2:n.416+1G>A
ENST00000452085.7:c.416+1G>A	ENSP00000404049.2:n.416+1G>A
ENST00000607094.1:n.1059G>A
ENST00000643175.1:c.417G>A	ENSP00000495885.1:p.Trp139Ter
ENST00000644499.1:c.272+1G>A	ENSP00000495266.1:n.272+1G>A
ENST00000646710.1:c.416+1G>A	ENSP00000495970.1:n.416+1G>A
ENST00000647244.1:c.416+1G>A	ENSP00000495184.1:n.416+1G>A
XM_011535785.1:c.-172+1G>A	XP_011534087.1:n.-172+1G>A
XM_017010795.1:c.473+1G>A	XP_016866284.1:n.473+1G>A
XM_017010796.1:c.416+1G>A	XP_016866285.1:n.416+1G>A
XM_017010797.1:c.473+1G>A	XP_016866286.1:n.473+1G>A