Canonical Allele Identifier: CA2565312627
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542862A>T , CM000680.2:g.31542862A>T GRCh38
NC_000018.9:g.29122825A>T , CM000680.1:g.29122825A>T GRCh37
NC_000018.8:g.27376823A>T NCBI36
NG_007072.3:g.49621A>T , LRG_397:g.49621A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2334+10A>T (DSG2) MANE Select ENSP00000261590.8:n.2334+10A>T
ENST00000261590.12:c.2334+10A>T (DSG2) ENSP00000261590.8:n.2334+10A>T
NM_001943.3:c.2334+10A>T , LRG_397t1:c.2334+10A>T (DSG2) NP_001934.2:n.2334+10A>T
NR_045216.1:n.1810+240T>A (DSG2-AS1)
NM_001943.4:c.2334+10A>T (DSG2) NP_001934.2:n.2334+10A>T
XM_024451095.1:c.1800+10A>T (DSG2) XP_024306863.1:n.1800+10A>T
NM_001943.5:c.2334+10A>T (DSG2) MANE Select NP_001934.2:n.2334+10A>T