Canonical Allele Identifier: CA2528091874
Gene: SHISA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11346930_11346931insGGT , CM000679.2:g.11346930_11346931insGGT GRCh38
NC_000017.10:g.11250247_11250248insGGT , CM000679.1:g.11250247_11250248insGGT GRCh37
NC_000017.9:g.11190972_11190973insGGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000441885.8:c.800-32484_800-32483insGGT MANE Select ENSP00000390084.3:n.800-32484_800-32483insGGT
ENST00000343478.7:c.282-32484_282-32483insGGT
ENST00000409168.7:c.799+83404_799+83405insGGT ENSP00000387157.3:n.799+83404_799+83405insGGT
ENST00000432116.7:c.800-32484_800-32483insGGT ENSP00000388659.3:n.800-32484_800-32483insGGT
ENST00000441885.7:c.800-32484_800-32483insGGT ENSP00000390084.3:n.800-32484_800-32483insGGT
NM_001173461.1:c.799+83404_799+83405insGGT NP_001166932.1:n.799+83404_799+83405insGGT
NM_001173462.1:c.800-32484_800-32483insGGT NP_001166933.1:n.800-32484_800-32483insGGT
NM_207386.3:c.800-32484_800-32483insGGT NP_997269.2:n.800-32484_800-32483insGGT
XM_011523837.1:c.800-32484_800-32483insGGT XP_011522139.1:n.800-32484_800-32483insGGT
XM_017024618.1:c.799+83404_799+83405insGGT XP_016880107.1:n.799+83404_799+83405insGGT
NM_001173462.2:c.800-32484_800-32483insGGT NP_001166933.1:n.800-32484_800-32483insGGT
NM_207386.4:c.800-32484_800-32483insGGT MANE Select NP_997269.2:n.800-32484_800-32483insGGT