Canonical Allele Identifier: CA16604128

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420823C>T , CM000664.2:g.219420823C>T	GRCh38
NC_000002.11:g.220285545C>T , CM000664.1:g.220285545C>T	GRCh37
NC_000002.10:g.219993789C>T	NCBI36
NG_008043.1:g.7447C>T , LRG_380:g.7447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.372-5C>T
ENST00000683013.1:n.286-5C>T
ENST00000373960.4:c.898-5C>T MANE Select	ENSP00000363071.3:n.898-5C>T
ENST00000373960.3:c.898-5C>T	ENSP00000363071.3:n.898-5C>T
ENST00000477226.5:n.370-5C>T
ENST00000492726.1:n.293-5C>T
NM_001927.3:c.898-5C>T , LRG_380t1:c.898-5C>T	NP_001918.3:n.898-5C>T
NM_001927.4:c.898-5C>T MANE Select	NP_001918.3:n.898-5C>T
NM_001382708.1:c.895-5C>T	NP_001369637.1:n.895-5C>T
NM_001382709.1:c.735+477C>T	NP_001369638.1:n.735+477C>T
NM_001382710.1:c.898-5C>T	NP_001369639.1:n.898-5C>T
NM_001382711.1:c.898-5C>T	NP_001369640.1:n.898-5C>T
NM_001382712.1:c.898-5C>T	NP_001369641.1:n.898-5C>T
NM_001382713.1:c.628-5C>T	NP_001369642.1:n.628-5C>T