Canonical Allele Identifier: CA1329210884

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420554G= , CM000664.2:g.219420554G=	GRCh38
NC_000002.11:g.220285276G= , CM000664.1:g.220285276G=	GRCh37
NC_000002.10:g.219993520G=	NCBI36
NG_008043.1:g.7178G= , LRG_380:g.7178G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.269G=
ENST00000683013.1:n.183G=
ENST00000373960.4:c.795G= MANE Select	ENSP00000363071.3:p.Met265=
ENST00000373960.3:c.795G=	ENSP00000363071.3:p.Met265=
ENST00000477226.5:n.267G=
ENST00000492726.1:n.190G=
NM_001927.3:c.795G= , LRG_380t1:c.795G=	NP_001918.3:p.Met265=
NM_001927.4:c.795G= MANE Select	NP_001918.3:p.Met265=
NM_001382708.1:c.792G=	NP_001369637.1:p.Met264=
NM_001382709.1:c.735+208G=	NP_001369638.1:n.735+208G=
NM_001382710.1:c.795G=	NP_001369639.1:p.Met265=
NM_001382711.1:c.795G=	NP_001369640.1:p.Met265=
NM_001382712.1:c.795G=	NP_001369641.1:p.Met265=
NM_001382713.1:c.525G=	NP_001369642.1:p.Met175=