Canonical Allele Identifier: CA1329210688

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420193C= , CM000664.2:g.219420193C=	GRCh38
NC_000002.11:g.220284915C= , CM000664.1:g.220284915C=	GRCh37
NC_000002.10:g.219993159C=	NCBI36
NG_008043.1:g.6817C= , LRG_380:g.6817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.113+38C=
ENST00000373960.4:c.639+38C= MANE Select	ENSP00000363071.3:n.639+38C=
ENST00000373960.3:c.639+38C=	ENSP00000363071.3:n.639+38C=
ENST00000477226.5:n.111+38C=
ENST00000492726.1:n.34+38C=
NM_001927.3:c.639+38C= , LRG_380t1:c.639+38C=	NP_001918.3:n.639+38C=
NM_001927.4:c.639+38C= MANE Select	NP_001918.3:n.639+38C=
NM_001382708.1:c.636+41C=	NP_001369637.1:n.636+41C=
NM_001382709.1:c.639+38C=	NP_001369638.1:n.639+38C=
NM_001382710.1:c.639+38C=	NP_001369639.1:n.639+38C=
NM_001382711.1:c.639+38C=	NP_001369640.1:n.639+38C=
NM_001382712.1:c.639+38C=	NP_001369641.1:n.639+38C=
NM_001382713.1:c.496-332C=	NP_001369642.1:n.496-332C=