Canonical Allele Identifier: CA350698611

Gene: DES

Linked Data

• gnomAD v4: 2-219425713-A-T
• MyVariant Identifiers: chr2:g.220290435A>T (hg19) ; chr2:g.219425713A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425713A>T , CM000664.2:g.219425713A>T	GRCh38
NC_000002.11:g.220290435A>T , CM000664.1:g.220290435A>T	GRCh37
NC_000002.10:g.219998679A>T	NCBI36
NG_008043.1:g.12337A>T , LRG_380:g.12337A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.813A>T
ENST00000683013.1:n.727A>T
ENST00000373960.4:c.1339A>T MANE Select	ENSP00000363071.3:p.Met447Leu
ENST00000373960.3:c.1339A>T	ENSP00000363071.3:p.Met447Leu
ENST00000483395.1:n.194A>T
NM_001927.3:c.1339A>T , LRG_380t1:c.1339A>T	NP_001918.3:p.Met447Leu
NM_001927.4:c.1339A>T MANE Select	NP_001918.3:p.Met447Leu
NM_001382708.1:c.1336A>T	NP_001369637.1:p.Met446Leu
NM_001382709.1:c.907A>T	NP_001369638.1:p.Met303Leu
NM_001382710.1:c.1270A>T	NP_001369639.1:p.Met424Leu
NM_001382711.1:c.1318A>T	NP_001369640.1:p.Met440Leu
NM_001382712.1:c.1339A>T	NP_001369641.1:p.Met447Leu
NM_001382713.1:c.1069A>T	NP_001369642.1:p.Met357Leu