Canonical Allele Identifier: CA350698276

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220290388C>G (hg19) ; chr2:g.219425666C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425666C>G , CM000664.2:g.219425666C>G	GRCh38
NC_000002.11:g.220290388C>G , CM000664.1:g.220290388C>G	GRCh37
NC_000002.10:g.219998632C>G	NCBI36
NG_008043.1:g.12290C>G , LRG_380:g.12290C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.766C>G
ENST00000683013.1:n.680C>G
ENST00000373960.4:c.1292C>G MANE Select	ENSP00000363071.3:p.Thr431Ser
ENST00000373960.3:c.1292C>G	ENSP00000363071.3:p.Thr431Ser
ENST00000483395.1:n.147C>G
NM_001927.3:c.1292C>G , LRG_380t1:c.1292C>G	NP_001918.3:p.Thr431Ser
NM_001927.4:c.1292C>G MANE Select	NP_001918.3:p.Thr431Ser
NM_001382708.1:c.1289C>G	NP_001369637.1:p.Thr430Ser
NM_001382709.1:c.860C>G	NP_001369638.1:p.Thr287Ser
NM_001382710.1:c.1223C>G	NP_001369639.1:p.Thr408Ser
NM_001382711.1:c.1271C>G	NP_001369640.1:p.Thr424Ser
NM_001382712.1:c.1292C>G	NP_001369641.1:p.Thr431Ser
NM_001382713.1:c.1022C>G	NP_001369642.1:p.Thr341Ser