Canonical Allele Identifier: CA2189596906

Gene: CHRNA5 CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78593646T= , CM000677.2:g.78593646T=	GRCh38
NC_000015.9:g.78885988T= , CM000677.1:g.78885988T=	GRCh37
NC_000015.8:g.76673043T=	NCBI36
NG_016143.1:g.32650A=
NG_023328.1:g.33127T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.*393T= (CHRNA5) MANE Select	ENSP00000299565.5:n.*393T=
ENST00000348639.7:c.1390-455A= (CHRNA3)	ENSP00000267951.4:n.1390-455A=
ENST00000559002.5:n.194-455A= (CHRNA3)
ENST00000559576.1:c.700T= (CHRNA5)
ENST00000559658.5:c.*162+268A= (CHRNA3)	ENSP00000452896.1:n.*162+268A=
NM_000745.3:c.*393T= (CHRNA5)	NP_000736.2:n.*393T=
NM_001166694.1:c.1390-455A= (CHRNA3)	NP_001160166.1:n.1390-455A=
NM_001307945.1:c.*530T= (CHRNA5)	NP_001294874.1:n.*530T=
NR_046313.1:n.2181+268A= (CHRNA3)
NM_001166694.2:c.1390-455A= (CHRNA3)	NP_001160166.1:n.1390-455A=
NM_001307945.2:c.*530T= (CHRNA5)	NP_001294874.1:n.*530T=
NR_046313.2:n.1882+268A= (CHRNA3)
NM_000745.4:c.*393T= (CHRNA5) MANE Select	NP_000736.2:n.*393T=
NM_001395171.1:c.*530T= (CHRNA5)	NP_001382100.1:n.*530T=
NM_001395172.1:c.*393T= (CHRNA5)	NP_001382101.1:n.*393T=
NM_001395173.1:c.*530T= (CHRNA5)	NP_001382102.1:n.*530T=
NM_001395174.1:c.*530T= (CHRNA5)	NP_001382103.1:n.*530T=
NM_001395175.1:c.*530T= (CHRNA5)	NP_001382104.1:n.*530T=