Canonical Allele Identifier: CA2293864137
Gene: DSG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541309G= , CM000680.2:g.31541309G= GRCh38
NC_000018.9:g.29121272G= , CM000680.1:g.29121272G= GRCh37
NC_000018.8:g.27375270G= NCBI36
NG_007072.3:g.48068G= , LRG_397:g.48068G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1996G= MANE Select ENSP00000261590.8:p.Asp666=
ENST00000261590.12:c.1996G= ENSP00000261590.8:p.Asp666=
NM_001943.3:c.1996G= , LRG_397t1:c.1996G= NP_001934.2:p.Asp666=
NM_001943.4:c.1996G= NP_001934.2:p.Asp666=
XM_024451095.1:c.1462G= XP_024306863.1:p.Asp488=
NM_001943.5:c.1996G= MANE Select NP_001934.2:p.Asp666=
Search 100 bp 5'
Search 100 bp 3'