Canonical Allele Identifier: CA402134221
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522256T>A , CM000680.2:g.31522256T>A GRCh38
NC_000018.9:g.29102219T>A , CM000680.1:g.29102219T>A GRCh37
NC_000018.8:g.27356217T>A NCBI36
NG_007072.3:g.29015T>A , LRG_397:g.29015T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.521+7T>A
ENST00000682241.2:c.690+7T>A ENSP00000507600.2:n.690+7T>A
ENST00000683614.2:n.521+7T>A
ENST00000682087.1:c.521+7T>A
ENST00000682241.1:c.521+7T>A
ENST00000683614.1:c.521+7T>A
ENST00000683654.1:c.690+7T>A ENSP00000506971.1:n.690+7T>A
ENST00000684461.1:n.1367T>A
ENST00000261590.13:c.690+7T>A MANE Select ENSP00000261590.8:n.690+7T>A
ENST00000261590.12:c.690+7T>A ENSP00000261590.8:n.690+7T>A
ENST00000585206.1:c.697T>A ENSP00000462503.1:p.Ter233Lys
NM_001943.3:c.690+7T>A , LRG_397t1:c.690+7T>A NP_001934.2:n.690+7T>A
NM_001943.4:c.690+7T>A NP_001934.2:n.690+7T>A
XM_024451095.1:c.156+7T>A XP_024306863.1:n.156+7T>A
NM_001943.5:c.690+7T>A MANE Select NP_001934.2:n.690+7T>A