Canonical Allele Identifier: CA350699139

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220290699A>C (hg19) ; chr2:g.219425977A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425977A>C , CM000664.2:g.219425977A>C	GRCh38
NC_000002.11:g.220290699A>C , CM000664.1:g.220290699A>C	GRCh37
NC_000002.10:g.219998943A>C	NCBI36
NG_008043.1:g.12601A>C , LRG_380:g.12601A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.874A>C
ENST00000683013.1:n.788A>C
ENST00000373960.4:c.1400A>C MANE Select	ENSP00000363071.3:p.His467Pro
ENST00000373960.3:c.1400A>C	ENSP00000363071.3:p.His467Pro
ENST00000483395.1:n.255A>C
NM_001927.3:c.1400A>C , LRG_380t1:c.1400A>C	NP_001918.3:p.His467Pro
NM_001927.4:c.1400A>C MANE Select	NP_001918.3:p.His467Pro
NM_001382708.1:c.1397A>C	NP_001369637.1:p.His466Pro
NM_001382709.1:c.968A>C	NP_001369638.1:p.His323Pro
NM_001382710.1:c.1331A>C	NP_001369639.1:p.His444Pro
NM_001382711.1:c.1379A>C	NP_001369640.1:p.His460Pro
NM_001382712.1:c.1371+232A>C	NP_001369641.1:n.1371+232A>C
NM_001382713.1:c.1130A>C	NP_001369642.1:p.His377Pro