Canonical Allele Identifier: CA2761148027
Gene: CHRNA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354490_40354491insCTTTCAGGTT , CM000666.2:g.40354490_40354491insCTTTCAGGTT GRCh38
NC_000004.11:g.40356507_40356508insCTTTCAGGTT , CM000666.1:g.40356507_40356508insCTTTCAGGTT GRCh37
NC_000004.10:g.40051264_40051265insCTTTCAGGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1410_1411insCTTTCAGGTT MANE Select ENSP00000312663.2:p.Thr471LeufsTer?
ENST00000310169.2:c.1410_1411insCTTTCAGGTT ENSP00000312663.2:p.Thr471LeufsTer?
NM_017581.3:c.1410_1411insCTTTCAGGTT NP_060051.2:p.Thr471LeufsTer?
NM_017581.4:c.1410_1411insCTTTCAGGTT MANE Select NP_060051.2:p.Thr471LeufsTer?