Canonical Allele Identifier: CA350695031

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286258A>T (hg19) ; chr2:g.219421536A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421536A>T , CM000664.2:g.219421536A>T	GRCh38
NC_000002.11:g.220286258A>T , CM000664.1:g.220286258A>T	GRCh37
NC_000002.10:g.219994502A>T	NCBI36
NG_008043.1:g.8160A>T , LRG_380:g.8160A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.694A>T
ENST00000683013.1:n.608A>T
ENST00000373960.4:c.1220A>T MANE Select	ENSP00000363071.3:p.Lys407Met
ENST00000373960.3:c.1220A>T	ENSP00000363071.3:p.Lys407Met
ENST00000477226.5:n.692A>T
ENST00000492726.1:n.615A>T
NM_001927.3:c.1220A>T , LRG_380t1:c.1220A>T	NP_001918.3:p.Lys407Met
NM_001927.4:c.1220A>T MANE Select	NP_001918.3:p.Lys407Met
NM_001382708.1:c.1217A>T	NP_001369637.1:p.Lys406Met
NM_001382709.1:c.788A>T	NP_001369638.1:p.Lys263Met
NM_001382710.1:c.1151A>T	NP_001369639.1:p.Lys384Met
NM_001382711.1:c.1199A>T	NP_001369640.1:p.Lys400Met
NM_001382712.1:c.1220A>T	NP_001369641.1:p.Lys407Met
NM_001382713.1:c.950A>T	NP_001369642.1:p.Lys317Met