Canonical Allele Identifier: CA1329211209

Gene: DES

Linked Data

• dbSNP Id: rs1954436263

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421308C>T , CM000664.2:g.219421308C>T	GRCh38
NC_000002.11:g.220286030C>T , CM000664.1:g.220286030C>T	GRCh37
NC_000002.10:g.219994274C>T	NCBI36
NG_008043.1:g.7932C>T , LRG_380:g.7932C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.498-32C>T
ENST00000683013.1:n.412-32C>T
ENST00000373960.4:c.1024-32C>T MANE Select	ENSP00000363071.3:n.1024-32C>T
ENST00000373960.3:c.1024-32C>T	ENSP00000363071.3:n.1024-32C>T
ENST00000477226.5:n.496-32C>T
ENST00000492726.1:n.419-32C>T
NM_001927.3:c.1024-32C>T , LRG_380t1:c.1024-32C>T	NP_001918.3:n.1024-32C>T
NM_001927.4:c.1024-32C>T MANE Select	NP_001918.3:n.1024-32C>T
NM_001382708.1:c.1021-32C>T	NP_001369637.1:n.1021-32C>T
NM_001382709.1:c.736-176C>T	NP_001369638.1:n.736-176C>T
NM_001382710.1:c.1024-101C>T	NP_001369639.1:n.1024-101C>T
NM_001382711.1:c.1024-53C>T	NP_001369640.1:n.1024-53C>T
NM_001382712.1:c.1024-32C>T	NP_001369641.1:n.1024-32C>T
NM_001382713.1:c.754-32C>T	NP_001369642.1:n.754-32C>T