Canonical Allele Identifier: CA431284475

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286229C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421507C>A , CM000664.2:g.219421507C>A	GRCh38
NC_000002.11:g.220286229C>A , CM000664.1:g.220286229C>A	GRCh37
NC_000002.10:g.219994473C>A	NCBI36
NG_008043.1:g.8131C>A , LRG_380:g.8131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.665C>A
ENST00000683013.1:n.579C>A
ENST00000373960.4:c.1191C>A MANE Select	ENSP00000363071.3:p.Ala397=
ENST00000373960.3:c.1191C>A	ENSP00000363071.3:p.Ala397=
ENST00000477226.5:n.663C>A
ENST00000492726.1:n.586C>A
NM_001927.3:c.1191C>A , LRG_380t1:c.1191C>A	NP_001918.3:p.Ala397=
NM_001927.4:c.1191C>A MANE Select	NP_001918.3:p.Ala397=
NM_001382708.1:c.1188C>A	NP_001369637.1:p.Ala396=
NM_001382709.1:c.759C>A	NP_001369638.1:p.Ala253=
NM_001382710.1:c.1122C>A	NP_001369639.1:p.Ala374=
NM_001382711.1:c.1170C>A	NP_001369640.1:p.Ala390=
NM_001382712.1:c.1191C>A	NP_001369641.1:p.Ala397=
NM_001382713.1:c.921C>A	NP_001369642.1:p.Ala307=