Canonical Allele Identifier: CA1329210659

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420154C= , CM000664.2:g.219420154C=	GRCh38
NC_000002.11:g.220284876C= , CM000664.1:g.220284876C=	GRCh37
NC_000002.10:g.219993120C=	NCBI36
NG_008043.1:g.6778C= , LRG_380:g.6778C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.112C=
ENST00000373960.4:c.638C= MANE Select	ENSP00000363071.3:p.Ala213=
ENST00000373960.3:c.638C=	ENSP00000363071.3:p.Ala213=
ENST00000477226.5:n.110C=
ENST00000492726.1:n.33C=
NM_001927.3:c.638C= , LRG_380t1:c.638C=	NP_001918.3:p.Ala213=
NM_001927.4:c.638C= MANE Select	NP_001918.3:p.Ala213=
NM_001382708.1:c.636+2C=	NP_001369637.1:n.636+2C=
NM_001382709.1:c.638C=	NP_001369638.1:p.Ala213=
NM_001382710.1:c.638C=	NP_001369639.1:p.Ala213=
NM_001382711.1:c.638C=	NP_001369640.1:p.Ala213=
NM_001382712.1:c.638C=	NP_001369641.1:p.Ala213=
NM_001382713.1:c.496-371C=	NP_001369642.1:n.496-371C=