Canonical Allele Identifier: CA2293861977
Gene: DSG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536335C= , CM000680.2:g.31536335C= GRCh38
NC_000018.9:g.29116298C= , CM000680.1:g.29116298C= GRCh37
NC_000018.8:g.27370296C= NCBI36
NG_007072.3:g.43094C= , LRG_397:g.43094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1557C= MANE Select ENSP00000261590.8:p.Asp519=
ENST00000261590.12:c.1557C= ENSP00000261590.8:p.Asp519=
NM_001943.3:c.1557C= , LRG_397t1:c.1557C= NP_001934.2:p.Asp519=
NM_001943.4:c.1557C= NP_001934.2:p.Asp519=
XM_024451095.1:c.1023C= XP_024306863.1:p.Asp341=
NM_001943.5:c.1557C= MANE Select NP_001934.2:p.Asp519=
Search 100 bp 5'
Search 100 bp 3'