Canonical Allele Identifier: CA431427438

Gene: DES

Linked Data

• dbSNP Id: rs1318299
• MyVariant Identifiers: chr2:g.220283259A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219418537A>C , CM000664.2:g.219418537A>C	GRCh38
NC_000002.11:g.220283259A>C , CM000664.1:g.220283259A>C	GRCh37
NC_000002.10:g.219991503A>C	NCBI36
NG_008043.1:g.5161A>C , LRG_380:g.5161A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373960.4:c.75A>C MANE Select	ENSP00000363071.3:p.Pro25=
ENST00000373960.3:c.75A>C	ENSP00000363071.3:p.Pro25=
NM_001927.3:c.75A>C , LRG_380t1:c.75A>C	NP_001918.3:p.Pro25=
NM_001927.4:c.75A>C MANE Select	NP_001918.3:p.Pro25=
NM_001382708.1:c.75A>C	NP_001369637.1:p.Pro25=
NM_001382709.1:c.75A>C	NP_001369638.1:p.Pro25=
NM_001382710.1:c.75A>C	NP_001369639.1:p.Pro25=
NM_001382711.1:c.75A>C	NP_001369640.1:p.Pro25=
NM_001382712.1:c.75A>C	NP_001369641.1:p.Pro25=
NM_001382713.1:c.75A>C	NP_001369642.1:p.Pro25=