Canonical Allele Identifier: CA2293864114
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541247C= , CM000680.2:g.31541247C= GRCh38
NC_000018.9:g.29121210C= , CM000680.1:g.29121210C= GRCh37
NC_000018.8:g.27375208C= NCBI36
NG_007072.3:g.48006C= , LRG_397:g.48006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1934C= MANE Select ENSP00000261590.8:p.Thr645=
ENST00000261590.12:c.1934C= ENSP00000261590.8:p.Thr645=
NM_001943.3:c.1934C= , LRG_397t1:c.1934C= NP_001934.2:p.Thr645=
NM_001943.4:c.1934C= NP_001934.2:p.Thr645=
XM_024451095.1:c.1400C= XP_024306863.1:p.Thr467=
NM_001943.5:c.1934C= MANE Select NP_001934.2:p.Thr645=
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