Canonical Allele Identifier: CA2293855822
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522032A= , CM000680.2:g.31522032A= GRCh38
NC_000018.9:g.29101995A= , CM000680.1:g.29101995A= GRCh37
NC_000018.8:g.27355993A= NCBI36
NG_007072.3:g.28791A= , LRG_397:g.28791A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.355-51A=
ENST00000682241.2:c.524-51A= ENSP00000507600.2:n.524-51A=
ENST00000683614.2:n.355-51A=
ENST00000682087.1:c.355-51A=
ENST00000682241.1:c.355-51A=
ENST00000683614.1:c.355-51A=
ENST00000683654.1:c.524-51A= ENSP00000506971.1:n.524-51A=
ENST00000684461.1:n.1143A=
ENST00000261590.13:c.524-51A= MANE Select ENSP00000261590.8:n.524-51A=
ENST00000261590.12:c.524-51A= ENSP00000261590.8:n.524-51A=
ENST00000585206.1:c.524-51A= ENSP00000462503.1:n.524-51A=
NM_001943.3:c.524-51A= , LRG_397t1:c.524-51A= NP_001934.2:n.524-51A=
NM_001943.4:c.524-51A= NP_001934.2:n.524-51A=
XM_024451095.1:c.-11-51A= XP_024306863.1:n.-11-51A=
NM_001943.5:c.524-51A= MANE Select NP_001934.2:n.524-51A=