Canonical Allele Identifier: CA2577252616

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421295A>G , CM000664.2:g.219421295A>G	GRCh38
NC_000002.11:g.220286017A>G , CM000664.1:g.220286017A>G	GRCh37
NC_000002.10:g.219994261A>G	NCBI36
NG_008043.1:g.7919A>G , LRG_380:g.7919A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.498-45A>G
ENST00000683013.1:n.412-45A>G
ENST00000373960.4:c.1024-45A>G MANE Select	ENSP00000363071.3:n.1024-45A>G
ENST00000373960.3:c.1024-45A>G	ENSP00000363071.3:n.1024-45A>G
ENST00000477226.5:n.496-45A>G
ENST00000492726.1:n.419-45A>G
NM_001927.3:c.1024-45A>G , LRG_380t1:c.1024-45A>G	NP_001918.3:n.1024-45A>G
NM_001927.4:c.1024-45A>G MANE Select	NP_001918.3:n.1024-45A>G
NM_001382708.1:c.1021-45A>G	NP_001369637.1:n.1021-45A>G
NM_001382709.1:c.736-189A>G	NP_001369638.1:n.736-189A>G
NM_001382710.1:c.1024-114A>G	NP_001369639.1:n.1024-114A>G
NM_001382711.1:c.1024-66A>G	NP_001369640.1:n.1024-66A>G
NM_001382712.1:c.1024-45A>G	NP_001369641.1:n.1024-45A>G
NM_001382713.1:c.754-45A>G	NP_001369642.1:n.754-45A>G