Canonical Allele Identifier: CA625158448
Gene: SHISA6 HGNC NCBI

Linked Data

dbSNP Id: rs1386766904

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11346989_11346994del , CM000679.2:g.11346989_11346994del GRCh38
NC_000017.10:g.11250306_11250311del , CM000679.1:g.11250306_11250311del GRCh37
NC_000017.9:g.11191031_11191036del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000441885.8:c.800-32425_800-32420del MANE Select ENSP00000390084.3:n.800-32425_800-32420del
ENST00000343478.7:c.282-32425_282-32420del
ENST00000409168.7:c.799+83463_799+83468del ENSP00000387157.3:n.799+83463_799+83468del
ENST00000432116.7:c.800-32425_800-32420del ENSP00000388659.3:n.800-32425_800-32420del
ENST00000441885.7:c.800-32425_800-32420del ENSP00000390084.3:n.800-32425_800-32420del
NM_001173461.1:c.799+83463_799+83468del NP_001166932.1:n.799+83463_799+83468del
NM_001173462.1:c.800-32425_800-32420del NP_001166933.1:n.800-32425_800-32420del
NM_207386.3:c.800-32425_800-32420del NP_997269.2:n.800-32425_800-32420del
XM_011523837.1:c.800-32425_800-32420del XP_011522139.1:n.800-32425_800-32420del
XM_017024618.1:c.799+83463_799+83468del XP_016880107.1:n.799+83463_799+83468del
NM_001173462.2:c.800-32425_800-32420del NP_001166933.1:n.800-32425_800-32420del
NM_207386.4:c.800-32425_800-32420del MANE Select NP_997269.2:n.800-32425_800-32420del