Canonical Allele Identifier: CA145885434

Gene: DSE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116435302C>G , CM000668.2:g.116435302C>G	GRCh38
NC_000006.11:g.116756465C>G , CM000668.1:g.116756465C>G	GRCh37
NC_000006.10:g.116863158C>G	NCBI36
NG_033266.1:g.160183C>G
NG_033266.3:g.186151C>G
NG_033266.4:g.186132C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_013352.4:c.1119-285C>G MANE Select	NP_037484.1:n.1119-285C>G
ENST00000644252.3:c.1119-285C>G MANE Select	ENSP00000494147.2:n.1119-285C>G
NM_001080976.1:c.1119-285C>G	NP_001074445.1:n.1119-285C>G
NM_001080976.2:c.1119-285C>G	NP_001074445.1:n.1119-285C>G
NM_001080976.3:c.1119-285C>G	NP_001074445.1:n.1119-285C>G
NM_001322937.1:c.1119-285C>G	NP_001309866.1:n.1119-285C>G
NM_001322937.2:c.1119-285C>G	NP_001309866.1:n.1119-285C>G
NM_001322938.1:c.1119-285C>G	NP_001309867.1:n.1119-285C>G
NM_001322938.2:c.1119-285C>G	NP_001309867.1:n.1119-285C>G
NM_001322939.1:c.1176-285C>G	NP_001309868.1:n.1176-285C>G
NM_001322939.2:c.1176-285C>G	NP_001309868.1:n.1176-285C>G
NM_001322940.1:c.558-285C>G	NP_001309869.1:n.558-285C>G
NM_001322940.2:c.558-285C>G	NP_001309869.1:n.558-285C>G
NM_001322941.1:c.558-285C>G	NP_001309870.1:n.558-285C>G
NM_001322941.2:c.558-285C>G	NP_001309870.1:n.558-285C>G
NM_001322943.1:c.671-285C>G	NP_001309872.1:n.671-285C>G
NM_001322943.2:c.671-285C>G	NP_001309872.1:n.671-285C>G
NM_001322944.1:c.911-285C>G	NP_001309873.1:n.911-285C>G
NM_001322944.2:c.911-285C>G	NP_001309873.1:n.911-285C>G
NM_001374520.1:c.120-285C>G	NP_001361449.1:n.120-285C>G
NM_001374521.1:c.84-285C>G	NP_001361450.1:n.84-285C>G
NM_013352.2:c.1119-285C>G	NP_037484.1:n.1119-285C>G
NM_013352.3:c.1119-285C>G	NP_037484.1:n.1119-285C>G
NR_136524.1:n.1158-285C>G
NR_136524.2:n.1135-285C>G
ENST00000331677.7:c.1119-285C>G	ENSP00000332151.2:n.1119-285C>G
ENST00000359564.2:c.1119-285C>G	ENSP00000352567.2:n.1119-285C>G
ENST00000359564.3:c.911-285C>G	ENSP00000352567.3:n.911-285C>G
ENST00000452085.7:c.1119-285C>G	ENSP00000404049.2:n.1119-285C>G
ENST00000606712.1:n.1023-285C>G
ENST00000644499.1:c.766+4109C>G	ENSP00000495266.1:n.766+4109C>G
ENST00000646710.1:c.671-285C>G	ENSP00000495970.1:n.671-285C>G
ENST00000647244.1:c.671-285C>G	ENSP00000495184.1:n.671-285C>G
XM_011535785.1:c.84-285C>G	XP_011534087.1:n.84-285C>G
XM_017010795.1:c.1176-285C>G	XP_016866284.1:n.1176-285C>G
XM_017010796.1:c.1119-285C>G	XP_016866285.1:n.1119-285C>G
XM_017010797.1:c.968-285C>G	XP_016866286.1:n.968-285C>G