Canonical Allele Identifier: CA2353123686
Gene: DSTN HGNC NCBI

Linked Data

dbSNP Id: rs2035393707
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.17585349del , CM000682.2:g.17585349del GRCh38
NC_000020.10:g.17565994del , CM000682.1:g.17565994del GRCh37
NC_000020.9:g.17513994del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000246069.12:c.3+15138del MANE Select ENSP00000246069.6:n.3+15138del
ENST00000246069.11:c.3+15138del ENSP00000246069.6:n.3+15138del
ENST00000449141.2:c.3+15138del ENSP00000434355.1:n.3+15138del
ENST00000474024.5:c.-180-6583del ENSP00000476975.1:n.-180-6583del
NM_001011546.1:c.-180-6583del NP_001011546.1:n.-180-6583del
NM_006870.3:c.3+15138del NP_006861.1:n.3+15138del
XM_011529142.1:c.3+15138del XP_011527444.1:n.3+15138del
XM_011529143.1:c.3+15138del XP_011527445.1:n.3+15138del
XM_011529144.1:c.-180-6583del XP_011527446.1:n.-180-6583del
NM_006870.4:c.3+15138del MANE Select NP_006861.1:n.3+15138del
NM_001011546.2:c.-180-6583del NP_001011546.1:n.-180-6583del
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