Canonical Allele Identifier: CA1329211371

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421585G= , CM000664.2:g.219421585G=	GRCh38
NC_000002.11:g.220286307G= , CM000664.1:g.220286307G=	GRCh37
NC_000002.10:g.219994551G=	NCBI36
NG_008043.1:g.8209G= , LRG_380:g.8209G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.718+25G=
ENST00000683013.1:n.632+25G=
ENST00000373960.4:c.1244+25G= MANE Select	ENSP00000363071.3:n.1244+25G=
ENST00000373960.3:c.1244+25G=	ENSP00000363071.3:n.1244+25G=
ENST00000477226.5:n.716+25G=
ENST00000492726.1:n.639+25G=
NM_001927.3:c.1244+25G= , LRG_380t1:c.1244+25G=	NP_001918.3:n.1244+25G=
NM_001927.4:c.1244+25G= MANE Select	NP_001918.3:n.1244+25G=
NM_001382708.1:c.1241+25G=	NP_001369637.1:n.1241+25G=
NM_001382709.1:c.812+25G=	NP_001369638.1:n.812+25G=
NM_001382710.1:c.1175+25G=	NP_001369639.1:n.1175+25G=
NM_001382711.1:c.1223+25G=	NP_001369640.1:n.1223+25G=
NM_001382712.1:c.1244+25G=	NP_001369641.1:n.1244+25G=
NM_001382713.1:c.974+25G=	NP_001369642.1:n.974+25G=