Canonical Allele Identifier: CA2629788252

Gene: CHRNA5

Linked Data

• gnomAD v4: 15-78586839-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78586839G>T , CM000677.2:g.78586839G>T	GRCh38
NC_000015.9:g.78879181G>T , CM000677.1:g.78879181G>T	GRCh37
NC_000015.8:g.76666236G>T	NCBI36
NG_023328.1:g.26320G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.303+150G>T MANE Select	ENSP00000299565.5:n.303+150G>T
ENST00000394802.4:c.118+150G>T
ENST00000559554.5:c.303+150G>T	ENSP00000453519.1:n.303+150G>T
NM_000745.3:c.303+150G>T	NP_000736.2:n.303+150G>T
NM_001307945.1:c.303+150G>T	NP_001294874.1:n.303+150G>T
XM_005254142.2:c.303+150G>T	XP_005254199.1:n.303+150G>T
NM_001307945.2:c.303+150G>T	NP_001294874.1:n.303+150G>T
NM_000745.4:c.303+150G>T MANE Select	NP_000736.2:n.303+150G>T
NM_001395171.1:c.303+150G>T	NP_001382100.1:n.303+150G>T
NM_001395172.1:c.303+150G>T	NP_001382101.1:n.303+150G>T
NM_001395173.1:c.303+150G>T	NP_001382102.1:n.303+150G>T
NM_001395174.1:c.303+150G>T	NP_001382103.1:n.303+150G>T
NM_001395175.1:c.300+150G>T	NP_001382104.1:n.300+150G>T