Canonical Allele Identifier: CA2293854950
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519806_31519808delinsTTA , CM000680.2:g.31519806_31519808delinsTTA GRCh38
NC_000018.9:g.29099769_29099771delinsTTA , CM000680.1:g.29099769_29099771delinsTTA GRCh37
NC_000018.8:g.27353767_27353769delinsTTA NCBI36
NG_007072.3:g.26565_26567delinsTTA , LRG_397:g.26565_26567delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000682241.2:c.85_87delinsTTA ENSP00000507600.2:p.Leu29=
ENST00000683654.1:c.85_87delinsTTA ENSP00000506971.1:p.Leu29=
ENST00000261590.13:c.85_87delinsTTA MANE Select ENSP00000261590.8:p.Leu29=
ENST00000261590.12:c.85_87delinsTTA ENSP00000261590.8:p.Leu29=
ENST00000585206.1:c.85_87delinsTTA ENSP00000462503.1:p.Leu29=
NM_001943.3:c.85_87delinsTTA , LRG_397t1:c.85_87delinsTTA NP_001934.2:p.Leu29=
NM_001943.4:c.85_87delinsTTA NP_001934.2:p.Leu29=
XM_024451095.1:c.-450_-448delinsTTA XP_024306863.1:n.-450_-448delinsTTA
NM_001943.5:c.85_87delinsTTA MANE Select NP_001934.2:p.Leu29=