Canonical Allele Identifier: CA1329211178

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421237G= , CM000664.2:g.219421237G=	GRCh38
NC_000002.11:g.220285959G= , CM000664.1:g.220285959G=	GRCh37
NC_000002.10:g.219994203G=	NCBI36
NG_008043.1:g.7861G= , LRG_380:g.7861G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.498-103G=
ENST00000683013.1:n.412-103G=
ENST00000373960.4:c.1024-103G= MANE Select	ENSP00000363071.3:n.1024-103G=
ENST00000373960.3:c.1024-103G=	ENSP00000363071.3:n.1024-103G=
ENST00000477226.5:n.496-103G=
ENST00000492726.1:n.419-103G=
NM_001927.3:c.1024-103G= , LRG_380t1:c.1024-103G=	NP_001918.3:n.1024-103G=
NM_001927.4:c.1024-103G= MANE Select	NP_001918.3:n.1024-103G=
NM_001382708.1:c.1021-103G=	NP_001369637.1:n.1021-103G=
NM_001382709.1:c.736-247G=	NP_001369638.1:n.736-247G=
NM_001382710.1:c.1024-172G=	NP_001369639.1:n.1024-172G=
NM_001382711.1:c.1024-124G=	NP_001369640.1:n.1024-124G=
NM_001382712.1:c.1024-103G=	NP_001369641.1:n.1024-103G=
NM_001382713.1:c.754-103G=	NP_001369642.1:n.754-103G=