Canonical Allele Identifier: CA350695135

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286282G>C (hg19) ; chr2:g.219421560G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421560G>C , CM000664.2:g.219421560G>C	GRCh38
NC_000002.11:g.220286282G>C , CM000664.1:g.220286282G>C	GRCh37
NC_000002.10:g.219994526G>C	NCBI36
NG_008043.1:g.8184G>C , LRG_380:g.8184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.718G>C
ENST00000683013.1:n.632G>C
ENST00000373960.4:c.1244G>C MANE Select	ENSP00000363071.3:p.Arg415Pro
ENST00000373960.3:c.1244G>C	ENSP00000363071.3:p.Arg415Pro
ENST00000477226.5:n.716G>C
ENST00000492726.1:n.639G>C
NM_001927.3:c.1244G>C , LRG_380t1:c.1244G>C	NP_001918.3:p.Arg415Pro
NM_001927.4:c.1244G>C MANE Select	NP_001918.3:p.Arg415Pro
NM_001382708.1:c.1241G>C	NP_001369637.1:p.Arg414Pro
NM_001382709.1:c.812G>C	NP_001369638.1:p.Arg271Pro
NM_001382710.1:c.1175G>C	NP_001369639.1:p.Arg392Pro
NM_001382711.1:c.1223G>C	NP_001369640.1:p.Arg408Pro
NM_001382712.1:c.1244G>C	NP_001369641.1:p.Arg415Pro
NM_001382713.1:c.974G>C	NP_001369642.1:p.Arg325Pro