Canonical Allele Identifier: CA350695039

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286260C>A (hg19) ; chr2:g.219421538C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421538C>A , CM000664.2:g.219421538C>A	GRCh38
NC_000002.11:g.220286260C>A , CM000664.1:g.220286260C>A	GRCh37
NC_000002.10:g.219994504C>A	NCBI36
NG_008043.1:g.8162C>A , LRG_380:g.8162C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.696C>A
ENST00000683013.1:n.610C>A
ENST00000373960.4:c.1222C>A MANE Select	ENSP00000363071.3:p.Leu408Met
ENST00000373960.3:c.1222C>A	ENSP00000363071.3:p.Leu408Met
ENST00000477226.5:n.694C>A
ENST00000492726.1:n.617C>A
NM_001927.3:c.1222C>A , LRG_380t1:c.1222C>A	NP_001918.3:p.Leu408Met
NM_001927.4:c.1222C>A MANE Select	NP_001918.3:p.Leu408Met
NM_001382708.1:c.1219C>A	NP_001369637.1:p.Leu407Met
NM_001382709.1:c.790C>A	NP_001369638.1:p.Leu264Met
NM_001382710.1:c.1153C>A	NP_001369639.1:p.Leu385Met
NM_001382711.1:c.1201C>A	NP_001369640.1:p.Leu401Met
NM_001382712.1:c.1222C>A	NP_001369641.1:p.Leu408Met
NM_001382713.1:c.952C>A	NP_001369642.1:p.Leu318Met