Canonical Allele Identifier: CA2293864112
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541246_31541247delinsAC , CM000680.2:g.31541246_31541247delinsAC GRCh38
NC_000018.9:g.29121209_29121210delinsAC , CM000680.1:g.29121209_29121210delinsAC GRCh37
NC_000018.8:g.27375207_27375208delinsAC NCBI36
NG_007072.3:g.48005_48006delinsAC , LRG_397:g.48005_48006delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1933_1934delinsAC MANE Select ENSP00000261590.8:p.Thr645=
ENST00000261590.12:c.1933_1934delinsAC ENSP00000261590.8:p.Thr645=
NM_001943.3:c.1933_1934delinsAC , LRG_397t1:c.1933_1934delinsAC NP_001934.2:p.Thr645=
NM_001943.4:c.1933_1934delinsAC NP_001934.2:p.Thr645=
XM_024451095.1:c.1399_1400delinsAC XP_024306863.1:p.Thr467=
NM_001943.5:c.1933_1934delinsAC MANE Select NP_001934.2:p.Thr645=
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