Canonical Allele Identifier: CA273899262

Gene: CHRNA5 CHRNA3

Linked Data

• dbSNP Id: rs923004974
• gnomAD v4: 15-78594620-G-A
• MyVariant Identifiers: chr15:g.78886962G>A (hg19) ; chr15:g.78594620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78594620G>A , CM000677.2:g.78594620G>A	GRCh38
NC_000015.9:g.78886962G>A , CM000677.1:g.78886962G>A	GRCh37
NC_000015.8:g.76674017G>A	NCBI36
NG_016143.1:g.31676C>T
NG_023328.1:g.34101G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.*1367G>A (CHRNA5) MANE Select	ENSP00000299565.5:n.*1367G>A
ENST00000348639.7:c.1390-1429C>T (CHRNA3)	ENSP00000267951.4:n.1390-1429C>T
ENST00000559002.5:n.194-1429C>T (CHRNA3)
ENST00000559658.5:c.*65-609C>T (CHRNA3)	ENSP00000452896.1:n.*65-609C>T
NM_000745.3:c.*1367G>A (CHRNA5)	NP_000736.2:n.*1367G>A
NM_001166694.1:c.1390-1429C>T (CHRNA3)	NP_001160166.1:n.1390-1429C>T
NM_001307945.1:c.*1504G>A (CHRNA5)	NP_001294874.1:n.*1504G>A
NR_046313.1:n.2084-609C>T (CHRNA3)
NM_001166694.2:c.1390-1429C>T (CHRNA3)	NP_001160166.1:n.1390-1429C>T
NM_001307945.2:c.*1504G>A (CHRNA5)	NP_001294874.1:n.*1504G>A
NR_046313.2:n.1785-609C>T (CHRNA3)
NM_000745.4:c.*1367G>A (CHRNA5) MANE Select	NP_000736.2:n.*1367G>A
NM_001395171.1:c.*1504G>A (CHRNA5)	NP_001382100.1:n.*1504G>A
NM_001395172.1:c.*1367G>A (CHRNA5)	NP_001382101.1:n.*1367G>A
NM_001395173.1:c.*1504G>A (CHRNA5)	NP_001382102.1:n.*1504G>A
NM_001395174.1:c.*1504G>A (CHRNA5)	NP_001382103.1:n.*1504G>A
NM_001395175.1:c.*1504G>A (CHRNA5)	NP_001382104.1:n.*1504G>A