Canonical Allele Identifier: CA2629784912

Gene: CHRNA5

Linked Data

• gnomAD v4: 15-78580790-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78580790T>C , CM000677.2:g.78580790T>C	GRCh38
NC_000015.9:g.78873132T>C , CM000677.1:g.78873132T>C	GRCh37
NC_000015.8:g.76660187T>C	NCBI36
NG_023328.1:g.20271T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.107-21T>C MANE Select	ENSP00000299565.5:n.107-21T>C
ENST00000559554.5:c.107-21T>C	ENSP00000453519.1:n.107-21T>C
NM_000745.3:c.107-21T>C	NP_000736.2:n.107-21T>C
NM_001307945.1:c.107-21T>C	NP_001294874.1:n.107-21T>C
XM_005254142.2:c.107-21T>C	XP_005254199.1:n.107-21T>C
NM_001307945.2:c.107-21T>C	NP_001294874.1:n.107-21T>C
NM_000745.4:c.107-21T>C MANE Select	NP_000736.2:n.107-21T>C
NM_001395171.1:c.107-21T>C	NP_001382100.1:n.107-21T>C
NM_001395172.1:c.107-21T>C	NP_001382101.1:n.107-21T>C
NM_001395173.1:c.107-21T>C	NP_001382102.1:n.107-21T>C
NM_001395174.1:c.107-21T>C	NP_001382103.1:n.107-21T>C
NM_001395175.1:c.107-21T>C	NP_001382104.1:n.107-21T>C