Canonical Allele Identifier: CA350698933

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220290672T>C (hg19) ; chr2:g.219425950T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425950T>C , CM000664.2:g.219425950T>C	GRCh38
NC_000002.11:g.220290672T>C , CM000664.1:g.220290672T>C	GRCh37
NC_000002.10:g.219998916T>C	NCBI36
NG_008043.1:g.12574T>C , LRG_380:g.12574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.847T>C
ENST00000683013.1:n.761T>C
ENST00000373960.4:c.1373T>C MANE Select	ENSP00000363071.3:p.Val458Ala
ENST00000373960.3:c.1373T>C	ENSP00000363071.3:p.Val458Ala
ENST00000483395.1:n.228T>C
NM_001927.3:c.1373T>C , LRG_380t1:c.1373T>C	NP_001918.3:p.Val458Ala
NM_001927.4:c.1373T>C MANE Select	NP_001918.3:p.Val458Ala
NM_001382708.1:c.1370T>C	NP_001369637.1:p.Val457Ala
NM_001382709.1:c.941T>C	NP_001369638.1:p.Val314Ala
NM_001382710.1:c.1304T>C	NP_001369639.1:p.Val435Ala
NM_001382711.1:c.1352T>C	NP_001369640.1:p.Val451Ala
NM_001382712.1:c.1371+205T>C	NP_001369641.1:n.1371+205T>C
NM_001382713.1:c.1103T>C	NP_001369642.1:p.Val368Ala