Canonical Allele Identifier: CA350691376

Gene: DES

Linked Data

• dbSNP Id: rs1459036752
• MyVariant Identifiers: chr2:g.220285311T>C (hg19) ; chr2:g.219420589T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420589T>C , CM000664.2:g.219420589T>C	GRCh38
NC_000002.11:g.220285311T>C , CM000664.1:g.220285311T>C	GRCh37
NC_000002.10:g.219993555T>C	NCBI36
NG_008043.1:g.7213T>C , LRG_380:g.7213T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.304T>C
ENST00000683013.1:n.218T>C
ENST00000373960.4:c.830T>C MANE Select	ENSP00000363071.3:p.Ile277Thr
ENST00000373960.3:c.830T>C	ENSP00000363071.3:p.Ile277Thr
ENST00000477226.5:n.302T>C
ENST00000492726.1:n.225T>C
NM_001927.3:c.830T>C , LRG_380t1:c.830T>C	NP_001918.3:p.Ile277Thr
NM_001927.4:c.830T>C MANE Select	NP_001918.3:p.Ile277Thr
NM_001382708.1:c.827T>C	NP_001369637.1:p.Ile276Thr
NM_001382709.1:c.735+243T>C	NP_001369638.1:n.735+243T>C
NM_001382710.1:c.830T>C	NP_001369639.1:p.Ile277Thr
NM_001382711.1:c.830T>C	NP_001369640.1:p.Ile277Thr
NM_001382712.1:c.830T>C	NP_001369641.1:p.Ile277Thr
NM_001382713.1:c.560T>C	NP_001369642.1:p.Ile187Thr