Canonical Allele Identifier: CA503598135
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29102107A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522144A>G , CM000680.2:g.31522144A>G GRCh38
NC_000018.9:g.29102107A>G , CM000680.1:g.29102107A>G GRCh37
NC_000018.8:g.27356105A>G NCBI36
NG_007072.3:g.28903A>G , LRG_397:g.28903A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.416A>G
ENST00000682241.2:c.585A>G ENSP00000507600.2:p.Lys195=
ENST00000683614.2:n.416A>G
ENST00000682087.1:c.416A>G
ENST00000682241.1:c.416A>G
ENST00000683614.1:c.416A>G
ENST00000683654.1:c.585A>G ENSP00000506971.1:p.Lys195=
ENST00000684461.1:n.1255A>G
ENST00000261590.13:c.585A>G MANE Select ENSP00000261590.8:p.Lys195=
ENST00000261590.12:c.585A>G ENSP00000261590.8:p.Lys195=
ENST00000585206.1:c.585A>G ENSP00000462503.1:p.Lys195=
NM_001943.3:c.585A>G , LRG_397t1:c.585A>G NP_001934.2:p.Lys195=
NM_001943.4:c.585A>G NP_001934.2:p.Lys195=
XM_024451095.1:c.51A>G XP_024306863.1:p.Lys17=
NM_001943.5:c.585A>G MANE Select NP_001934.2:p.Lys195=