Canonical Allele Identifier: CA431284304

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286133C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421411C>T , CM000664.2:g.219421411C>T	GRCh38
NC_000002.11:g.220286133C>T , CM000664.1:g.220286133C>T	GRCh37
NC_000002.10:g.219994377C>T	NCBI36
NG_008043.1:g.8035C>T , LRG_380:g.8035C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.569C>T
ENST00000683013.1:n.483C>T
ENST00000373960.4:c.1095C>T MANE Select	ENSP00000363071.3:p.Asp365=
ENST00000373960.3:c.1095C>T	ENSP00000363071.3:p.Asp365=
ENST00000477226.5:n.567C>T
ENST00000492726.1:n.490C>T
NM_001927.3:c.1095C>T , LRG_380t1:c.1095C>T	NP_001918.3:p.Asp365=
NM_001927.4:c.1095C>T MANE Select	NP_001918.3:p.Asp365=
NM_001382708.1:c.1092C>T	NP_001369637.1:p.Asp364=
NM_001382709.1:c.736-73C>T	NP_001369638.1:n.736-73C>T
NM_001382710.1:c.1026C>T	NP_001369639.1:p.Asp342=
NM_001382711.1:c.1074C>T	NP_001369640.1:p.Asp358=
NM_001382712.1:c.1095C>T	NP_001369641.1:p.Asp365=
NM_001382713.1:c.825C>T	NP_001369642.1:p.Asp275=