Canonical Allele Identifier: CA2293854951
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519807T= , CM000680.2:g.31519807T= GRCh38
NC_000018.9:g.29099770T= , CM000680.1:g.29099770T= GRCh37
NC_000018.8:g.27353768T= NCBI36
NG_007072.3:g.26566T= , LRG_397:g.26566T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.86T= ENSP00000507600.2:p.Leu29=
ENST00000683654.1:c.86T= ENSP00000506971.1:p.Leu29=
ENST00000261590.13:c.86T= MANE Select ENSP00000261590.8:p.Leu29=
ENST00000261590.12:c.86T= ENSP00000261590.8:p.Leu29=
ENST00000585206.1:c.86T= ENSP00000462503.1:p.Leu29=
NM_001943.3:c.86T= , LRG_397t1:c.86T= NP_001934.2:p.Leu29=
NM_001943.4:c.86T= NP_001934.2:p.Leu29=
XM_024451095.1:c.-449T= XP_024306863.1:n.-449T=
NM_001943.5:c.86T= MANE Select NP_001934.2:p.Leu29=