Canonical Allele Identifier: CA2293866099
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546262A= , CM000680.2:g.31546262A= GRCh38
NC_000018.9:g.29126225A= , CM000680.1:g.29126225A= GRCh37
NC_000018.8:g.27380223A= NCBI36
NG_007072.3:g.53021A= , LRG_397:g.53021A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2876A= (DSG2) MANE Select ENSP00000261590.8:p.Gln959=
ENST00000261590.12:c.2876A= (DSG2) ENSP00000261590.8:p.Gln959=
NM_001943.3:c.2876A= , LRG_397t1:c.2876A= (DSG2) NP_001934.2:p.Gln959=
NR_045216.1:n.1346-356T= (DSG2-AS1)
NM_001943.4:c.2876A= (DSG2) NP_001934.2:p.Gln959=
XM_024451095.1:c.2342A= (DSG2) XP_024306863.1:p.Gln781=
NM_001943.5:c.2876A= (DSG2) MANE Select NP_001934.2:p.Gln959=