Canonical Allele Identifier: CA2293864651
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542692T= , CM000680.2:g.31542692T= GRCh38
NC_000018.9:g.29122655T= , CM000680.1:g.29122655T= GRCh37
NC_000018.8:g.27376653T= NCBI36
NG_007072.3:g.49451T= , LRG_397:g.49451T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2174T= (DSG2) MANE Select ENSP00000261590.8:p.Leu725=
ENST00000261590.12:c.2174T= (DSG2) ENSP00000261590.8:p.Leu725=
NM_001943.3:c.2174T= , LRG_397t1:c.2174T= (DSG2) NP_001934.2:p.Leu725=
NR_045216.1:n.1811-371A= (DSG2-AS1)
NM_001943.4:c.2174T= (DSG2) NP_001934.2:p.Leu725=
XM_024451095.1:c.1640T= (DSG2) XP_024306863.1:p.Leu547=
NM_001943.5:c.2174T= (DSG2) MANE Select NP_001934.2:p.Leu725=