Canonical Allele Identifier: CA2695227364
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546024_31546025delinsC , CM000680.2:g.31546024_31546025delinsC GRCh38
NC_000018.9:g.29125987_29125988delinsC , CM000680.1:g.29125987_29125988delinsC GRCh37
NC_000018.8:g.27379985_27379986delinsC NCBI36
NG_007072.3:g.52783_52784delinsC , LRG_397:g.52783_52784delinsC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2638_2639delinsC (DSG2) MANE Select ENSP00000261590.8:p.Asn880LeufsTer23
ENST00000261590.12:c.2638_2639delinsC (DSG2) ENSP00000261590.8:p.Asn880LeufsTer23
NM_001943.3:c.2638_2639delinsC , LRG_397t1:c.2638_2639delinsC (DSG2) NP_001934.2:p.Asn880LeufsTer23
NR_045216.1:n.1346-119_1346-118delinsG (DSG2-AS1)
NM_001943.4:c.2638_2639delinsC (DSG2) NP_001934.2:p.Asn880LeufsTer23
XM_024451095.1:c.2104_2105delinsC (DSG2) XP_024306863.1:p.Asn702LeufsTer23
NM_001943.5:c.2638_2639delinsC (DSG2) MANE Select NP_001934.2:p.Asn880LeufsTer23