Canonical Allele Identifier: CA350694485

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286174A>C (hg19) ; chr2:g.219421452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421452A>C , CM000664.2:g.219421452A>C	GRCh38
NC_000002.11:g.220286174A>C , CM000664.1:g.220286174A>C	GRCh37
NC_000002.10:g.219994418A>C	NCBI36
NG_008043.1:g.8076A>C , LRG_380:g.8076A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.610A>C
ENST00000683013.1:n.524A>C
ENST00000373960.4:c.1136A>C MANE Select	ENSP00000363071.3:p.Asp379Ala
ENST00000373960.3:c.1136A>C	ENSP00000363071.3:p.Asp379Ala
ENST00000477226.5:n.608A>C
ENST00000492726.1:n.531A>C
NM_001927.3:c.1136A>C , LRG_380t1:c.1136A>C	NP_001918.3:p.Asp379Ala
NM_001927.4:c.1136A>C MANE Select	NP_001918.3:p.Asp379Ala
NM_001382708.1:c.1133A>C	NP_001369637.1:p.Asp378Ala
NM_001382709.1:c.736-32A>C	NP_001369638.1:n.736-32A>C
NM_001382710.1:c.1067A>C	NP_001369639.1:p.Asp356Ala
NM_001382711.1:c.1115A>C	NP_001369640.1:p.Asp372Ala
NM_001382712.1:c.1136A>C	NP_001369641.1:p.Asp379Ala
NM_001382713.1:c.866A>C	NP_001369642.1:p.Asp289Ala