Canonical Allele Identifier: CA1329211172

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421228G= , CM000664.2:g.219421228G=	GRCh38
NC_000002.11:g.220285950G= , CM000664.1:g.220285950G=	GRCh37
NC_000002.10:g.219994194G=	NCBI36
NG_008043.1:g.7852G= , LRG_380:g.7852G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.498-112G=
ENST00000683013.1:n.412-112G=
ENST00000373960.4:c.1024-112G= MANE Select	ENSP00000363071.3:n.1024-112G=
ENST00000373960.3:c.1024-112G=	ENSP00000363071.3:n.1024-112G=
ENST00000477226.5:n.496-112G=
ENST00000492726.1:n.419-112G=
NM_001927.3:c.1024-112G= , LRG_380t1:c.1024-112G=	NP_001918.3:n.1024-112G=
NM_001927.4:c.1024-112G= MANE Select	NP_001918.3:n.1024-112G=
NM_001382708.1:c.1021-112G=	NP_001369637.1:n.1021-112G=
NM_001382709.1:c.736-256G=	NP_001369638.1:n.736-256G=
NM_001382710.1:c.1024-181G=	NP_001369639.1:n.1024-181G=
NM_001382711.1:c.1024-133G=	NP_001369640.1:n.1024-133G=
NM_001382712.1:c.1024-112G=	NP_001369641.1:n.1024-112G=
NM_001382713.1:c.754-112G=	NP_001369642.1:n.754-112G=