Canonical Allele Identifier: CA402148721
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126501T>A (hg19) chr18:g.31546538T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546538T>A , CM000680.2:g.31546538T>A GRCh38
NC_000018.9:g.29126501T>A , CM000680.1:g.29126501T>A GRCh37
NC_000018.8:g.27380499T>A NCBI36
NG_007072.3:g.53297T>A , LRG_397:g.53297T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3152T>A (DSG2) MANE Select ENSP00000261590.8:p.Leu1051Gln
ENST00000261590.12:c.3152T>A (DSG2) ENSP00000261590.8:p.Leu1051Gln
NM_001943.3:c.3152T>A , LRG_397t1:c.3152T>A (DSG2) NP_001934.2:p.Leu1051Gln
NR_045216.1:n.1346-632A>T (DSG2-AS1)
NM_001943.4:c.3152T>A (DSG2) NP_001934.2:p.Leu1051Gln
XM_024451095.1:c.2618T>A (DSG2) XP_024306863.1:p.Leu873Gln
NM_001943.5:c.3152T>A (DSG2) MANE Select NP_001934.2:p.Leu1051Gln
Search 100 bp 5'
Search 100 bp 3'