Canonical Allele Identifier: CA2843661281

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420453dup , CM000664.2:g.219420453dup	GRCh38
NC_000002.11:g.220285175dup , CM000664.1:g.220285175dup	GRCh37
NC_000002.10:g.219993419dup	NCBI36
NG_008043.1:g.7077dup , LRG_380:g.7077dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.210-42dup
ENST00000683013.1:n.124-42dup
ENST00000373960.4:c.736-42dup MANE Select	ENSP00000363071.3:n.736-42dup
ENST00000373960.3:c.736-42dup	ENSP00000363071.3:n.736-42dup
ENST00000477226.5:n.208-42dup
ENST00000492726.1:n.131-42dup
NM_001927.3:c.736-42dup , LRG_380t1:c.736-42dup	NP_001918.3:n.736-42dup
NM_001927.4:c.736-42dup MANE Select	NP_001918.3:n.736-42dup
NM_001382708.1:c.733-42dup	NP_001369637.1:n.733-42dup
NM_001382709.1:c.735+107dup	NP_001369638.1:n.735+107dup
NM_001382710.1:c.736-42dup	NP_001369639.1:n.736-42dup
NM_001382711.1:c.736-42dup	NP_001369640.1:n.736-42dup
NM_001382712.1:c.736-42dup	NP_001369641.1:n.736-42dup
NM_001382713.1:c.496-72dup	NP_001369642.1:n.496-72dup