Canonical Allele Identifier: CA402148543
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546505T>G , CM000680.2:g.31546505T>G GRCh38
NC_000018.9:g.29126468T>G , CM000680.1:g.29126468T>G GRCh37
NC_000018.8:g.27380466T>G NCBI36
NG_007072.3:g.53264T>G , LRG_397:g.53264T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3119T>G (DSG2) MANE Select ENSP00000261590.8:p.Val1040Gly
ENST00000261590.12:c.3119T>G (DSG2) ENSP00000261590.8:p.Val1040Gly
NM_001943.3:c.3119T>G , LRG_397t1:c.3119T>G (DSG2) NP_001934.2:p.Val1040Gly
NR_045216.1:n.1346-599A>C (DSG2-AS1)
NM_001943.4:c.3119T>G (DSG2) NP_001934.2:p.Val1040Gly
XM_024451095.1:c.2585T>G (DSG2) XP_024306863.1:p.Val862Gly
NM_001943.5:c.3119T>G (DSG2) MANE Select NP_001934.2:p.Val1040Gly