Canonical Allele Identifier: CA2293864155
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541354G= , CM000680.2:g.31541354G= GRCh38
NC_000018.9:g.29121317G= , CM000680.1:g.29121317G= GRCh37
NC_000018.8:g.27375315G= NCBI36
NG_007072.3:g.48113G= , LRG_397:g.48113G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2001+40G= MANE Select ENSP00000261590.8:n.2001+40G=
ENST00000261590.12:c.2001+40G= ENSP00000261590.8:n.2001+40G=
NM_001943.3:c.2001+40G= , LRG_397t1:c.2001+40G= NP_001934.2:n.2001+40G=
NM_001943.4:c.2001+40G= NP_001934.2:n.2001+40G=
XM_024451095.1:c.1467+40G= XP_024306863.1:n.1467+40G=
NM_001943.5:c.2001+40G= MANE Select NP_001934.2:n.2001+40G=