Canonical Allele Identifier: CA2293864163
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541371_31541372delinsAG , CM000680.2:g.31541371_31541372delinsAG GRCh38
NC_000018.9:g.29121334_29121335delinsAG , CM000680.1:g.29121334_29121335delinsAG GRCh37
NC_000018.8:g.27375332_27375333delinsAG NCBI36
NG_007072.3:g.48130_48131delinsAG , LRG_397:g.48130_48131delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2001+57_2001+58delinsAG MANE Select ENSP00000261590.8:n.2001+57_2001+58delinsAG
ENST00000261590.12:c.2001+57_2001+58delinsAG ENSP00000261590.8:n.2001+57_2001+58delinsAG
NM_001943.3:c.2001+57_2001+58delinsAG , LRG_397t1:c.2001+57_2001+58delinsAG NP_001934.2:n.2001+57_2001+58delinsAG
NM_001943.4:c.2001+57_2001+58delinsAG NP_001934.2:n.2001+57_2001+58delinsAG
XM_024451095.1:c.1467+57_1467+58delinsAG XP_024306863.1:n.1467+57_1467+58delinsAG
NM_001943.5:c.2001+57_2001+58delinsAG MANE Select NP_001934.2:n.2001+57_2001+58delinsAG