Canonical Allele Identifier: CA431284465

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286209C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421487C>T , CM000664.2:g.219421487C>T	GRCh38
NC_000002.11:g.220286209C>T , CM000664.1:g.220286209C>T	GRCh37
NC_000002.10:g.219994453C>T	NCBI36
NG_008043.1:g.8111C>T , LRG_380:g.8111C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.645C>T
ENST00000683013.1:n.559C>T
ENST00000373960.4:c.1171C>T MANE Select	ENSP00000363071.3:p.Leu391=
ENST00000373960.3:c.1171C>T	ENSP00000363071.3:p.Leu391=
ENST00000477226.5:n.643C>T
ENST00000492726.1:n.566C>T
NM_001927.3:c.1171C>T , LRG_380t1:c.1171C>T	NP_001918.3:p.Leu391=
NM_001927.4:c.1171C>T MANE Select	NP_001918.3:p.Leu391=
NM_001382708.1:c.1168C>T	NP_001369637.1:p.Leu390=
NM_001382709.1:c.739C>T	NP_001369638.1:p.Leu247=
NM_001382710.1:c.1102C>T	NP_001369639.1:p.Leu368=
NM_001382711.1:c.1150C>T	NP_001369640.1:p.Leu384=
NM_001382712.1:c.1171C>T	NP_001369641.1:p.Leu391=
NM_001382713.1:c.901C>T	NP_001369642.1:p.Leu301=