Canonical Allele Identifier: CA2629788623
Gene: CHRNA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78590678dup , CM000677.2:g.78590678dup GRCh38
NC_000015.9:g.78883020dup , CM000677.1:g.78883020dup GRCh37
NC_000015.8:g.76670075dup NCBI36
NG_023328.1:g.30159dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.1245+42dup MANE Select ENSP00000299565.5:n.1245+42dup
ENST00000394802.4:c.522+580dup
ENST00000559554.5:c.458+829dup ENSP00000453519.1:n.458+829dup
ENST00000559576.1:c.145+172dup
NM_000745.3:c.1245+42dup NP_000736.2:n.1245+42dup
NM_001307945.1:c.458+829dup NP_001294874.1:n.458+829dup
XM_005254142.2:c.707+580dup XP_005254199.1:n.707+580dup
NM_001307945.2:c.458+829dup NP_001294874.1:n.458+829dup
NM_000745.4:c.1245+42dup MANE Select NP_000736.2:n.1245+42dup
NM_001395171.1:c.1115+172dup NP_001382100.1:n.1115+172dup
NM_001395172.1:c.591+696dup NP_001382101.1:n.591+696dup
NM_001395173.1:c.713+574dup NP_001382102.1:n.713+574dup
NM_001395174.1:c.707+580dup NP_001382103.1:n.707+580dup
NM_001395175.1:c.455+829dup NP_001382104.1:n.455+829dup