Canonical Allele Identifier: CA1329213080

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425624G= , CM000664.2:g.219425624G=	GRCh38
NC_000002.11:g.220290346G= , CM000664.1:g.220290346G=	GRCh37
NC_000002.10:g.219998590G=	NCBI36
NG_008043.1:g.12248G= , LRG_380:g.12248G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.763-39G=
ENST00000683013.1:n.677-39G=
ENST00000373960.4:c.1289-39G= MANE Select	ENSP00000363071.3:n.1289-39G=
ENST00000373960.3:c.1289-39G=	ENSP00000363071.3:n.1289-39G=
ENST00000483395.1:n.105G=
NM_001927.3:c.1289-39G= , LRG_380t1:c.1289-39G=	NP_001918.3:n.1289-39G=
NM_001927.4:c.1289-39G= MANE Select	NP_001918.3:n.1289-39G=
NM_001382708.1:c.1286-39G=	NP_001369637.1:n.1286-39G=
NM_001382709.1:c.857-39G=	NP_001369638.1:n.857-39G=
NM_001382710.1:c.1220-39G=	NP_001369639.1:n.1220-39G=
NM_001382711.1:c.1268-39G=	NP_001369640.1:n.1268-39G=
NM_001382712.1:c.1289-39G=	NP_001369641.1:n.1289-39G=
NM_001382713.1:c.1019-39G=	NP_001369642.1:n.1019-39G=