Canonical Allele Identifier: CA2189591959
Gene: CHRNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78589452_78589453delinsAG , CM000677.2:g.78589452_78589453delinsAG GRCh38
NC_000015.9:g.78881794_78881795delinsAG , CM000677.1:g.78881794_78881795delinsAG GRCh37
NC_000015.8:g.76668849_76668850delinsAG NCBI36
NG_023328.1:g.28933_28934delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.414-353_414-352delinsAG MANE Select ENSP00000299565.5:n.414-353_414-352delinsAG
ENST00000394802.4:c.229-353_229-352delinsAG
ENST00000559554.5:c.414-353_414-352delinsAG ENSP00000453519.1:n.414-353_414-352delinsAG
NM_000745.3:c.414-353_414-352delinsAG NP_000736.2:n.414-353_414-352delinsAG
NM_001307945.1:c.414-353_414-352delinsAG NP_001294874.1:n.414-353_414-352delinsAG
XM_005254142.2:c.414-353_414-352delinsAG XP_005254199.1:n.414-353_414-352delinsAG
NM_001307945.2:c.414-353_414-352delinsAG NP_001294874.1:n.414-353_414-352delinsAG
NM_000745.4:c.414-353_414-352delinsAG MANE Select NP_000736.2:n.414-353_414-352delinsAG
NM_001395171.1:c.414-353_414-352delinsAG NP_001382100.1:n.414-353_414-352delinsAG
NM_001395172.1:c.414-353_414-352delinsAG NP_001382101.1:n.414-353_414-352delinsAG
NM_001395173.1:c.414-353_414-352delinsAG NP_001382102.1:n.414-353_414-352delinsAG
NM_001395174.1:c.414-353_414-352delinsAG NP_001382103.1:n.414-353_414-352delinsAG
NM_001395175.1:c.411-353_411-352delinsAG NP_001382104.1:n.411-353_411-352delinsAG