Canonical Allele Identifier: CA350690727

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220285221T>C (hg19) ; chr2:g.219420499T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420499T>C , CM000664.2:g.219420499T>C	GRCh38
NC_000002.11:g.220285221T>C , CM000664.1:g.220285221T>C	GRCh37
NC_000002.10:g.219993465T>C	NCBI36
NG_008043.1:g.7123T>C , LRG_380:g.7123T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.214T>C
ENST00000683013.1:n.128T>C
ENST00000373960.4:c.740T>C MANE Select	ENSP00000363071.3:p.Ile247Thr
ENST00000373960.3:c.740T>C	ENSP00000363071.3:p.Ile247Thr
ENST00000477226.5:n.212T>C
ENST00000492726.1:n.135T>C
NM_001927.3:c.740T>C , LRG_380t1:c.740T>C	NP_001918.3:p.Ile247Thr
NM_001927.4:c.740T>C MANE Select	NP_001918.3:p.Ile247Thr
NM_001382708.1:c.737T>C	NP_001369637.1:p.Ile246Thr
NM_001382709.1:c.735+153T>C	NP_001369638.1:n.735+153T>C
NM_001382710.1:c.740T>C	NP_001369639.1:p.Ile247Thr
NM_001382711.1:c.740T>C	NP_001369640.1:p.Ile247Thr
NM_001382712.1:c.740T>C	NP_001369641.1:p.Ile247Thr
NM_001382713.1:c.496-26T>C	NP_001369642.1:n.496-26T>C