Canonical Allele Identifier: CA350694808

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286216A>C (hg19) ; chr2:g.219421494A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421494A>C , CM000664.2:g.219421494A>C	GRCh38
NC_000002.11:g.220286216A>C , CM000664.1:g.220286216A>C	GRCh37
NC_000002.10:g.219994460A>C	NCBI36
NG_008043.1:g.8118A>C , LRG_380:g.8118A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.652A>C
ENST00000683013.1:n.566A>C
ENST00000373960.4:c.1178A>C MANE Select	ENSP00000363071.3:p.Asn393Thr
ENST00000373960.3:c.1178A>C	ENSP00000363071.3:p.Asn393Thr
ENST00000477226.5:n.650A>C
ENST00000492726.1:n.573A>C
NM_001927.3:c.1178A>C , LRG_380t1:c.1178A>C	NP_001918.3:p.Asn393Thr
NM_001927.4:c.1178A>C MANE Select	NP_001918.3:p.Asn393Thr
NM_001382708.1:c.1175A>C	NP_001369637.1:p.Asn392Thr
NM_001382709.1:c.746A>C	NP_001369638.1:p.Asn249Thr
NM_001382710.1:c.1109A>C	NP_001369639.1:p.Asn370Thr
NM_001382711.1:c.1157A>C	NP_001369640.1:p.Asn386Thr
NM_001382712.1:c.1178A>C	NP_001369641.1:p.Asn393Thr
NM_001382713.1:c.908A>C	NP_001369642.1:p.Asn303Thr