Canonical Allele Identifier: CA2293866088
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546239G= , CM000680.2:g.31546239G= GRCh38
NC_000018.9:g.29126202G= , CM000680.1:g.29126202G= GRCh37
NC_000018.8:g.27380200G= NCBI36
NG_007072.3:g.52998G= , LRG_397:g.52998G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2853G= (DSG2) MANE Select ENSP00000261590.8:p.Val951=
ENST00000261590.12:c.2853G= (DSG2) ENSP00000261590.8:p.Val951=
NM_001943.3:c.2853G= , LRG_397t1:c.2853G= (DSG2) NP_001934.2:p.Val951=
NR_045216.1:n.1346-333C= (DSG2-AS1)
NM_001943.4:c.2853G= (DSG2) NP_001934.2:p.Val951=
XM_024451095.1:c.2319G= (DSG2) XP_024306863.1:p.Val773=
NM_001943.5:c.2853G= (DSG2) MANE Select NP_001934.2:p.Val951=
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