Canonical Allele Identifier: CA2247660684
Gene: SHISA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11346986T= , CM000679.2:g.11346986T= GRCh38
NC_000017.10:g.11250303T= , CM000679.1:g.11250303T= GRCh37
NC_000017.9:g.11191028T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000441885.8:c.800-32428T= MANE Select ENSP00000390084.3:n.800-32428T=
ENST00000343478.7:c.282-32428T=
ENST00000409168.7:c.799+83460T= ENSP00000387157.3:n.799+83460T=
ENST00000432116.7:c.800-32428T= ENSP00000388659.3:n.800-32428T=
ENST00000441885.7:c.800-32428T= ENSP00000390084.3:n.800-32428T=
NM_001173461.1:c.799+83460T= NP_001166932.1:n.799+83460T=
NM_001173462.1:c.800-32428T= NP_001166933.1:n.800-32428T=
NM_207386.3:c.800-32428T= NP_997269.2:n.800-32428T=
XM_011523837.1:c.800-32428T= XP_011522139.1:n.800-32428T=
XM_017024618.1:c.799+83460T= XP_016880107.1:n.799+83460T=
NM_001173462.2:c.800-32428T= NP_001166933.1:n.800-32428T=
NM_207386.4:c.800-32428T= MANE Select NP_997269.2:n.800-32428T=