Canonical Allele Identifier: CA2629788516

Gene: CHRNA5

Linked Data

• gnomAD v4: 15-78589423-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78589423_78589424insTC , CM000677.2:g.78589423_78589424insTC	GRCh38
NC_000015.9:g.78881765_78881766insTC , CM000677.1:g.78881765_78881766insTC	GRCh37
NC_000015.8:g.76668820_76668821insTC	NCBI36
NG_023328.1:g.28904_28905insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.414-382_414-381insTC MANE Select	ENSP00000299565.5:n.414-382_414-381insTC
ENST00000394802.4:c.229-382_229-381insTC
ENST00000559554.5:c.414-382_414-381insTC	ENSP00000453519.1:n.414-382_414-381insTC
NM_000745.3:c.414-382_414-381insTC	NP_000736.2:n.414-382_414-381insTC
NM_001307945.1:c.414-382_414-381insTC	NP_001294874.1:n.414-382_414-381insTC
XM_005254142.2:c.414-382_414-381insTC	XP_005254199.1:n.414-382_414-381insTC
NM_001307945.2:c.414-382_414-381insTC	NP_001294874.1:n.414-382_414-381insTC
NM_000745.4:c.414-382_414-381insTC MANE Select	NP_000736.2:n.414-382_414-381insTC
NM_001395171.1:c.414-382_414-381insTC	NP_001382100.1:n.414-382_414-381insTC
NM_001395172.1:c.414-382_414-381insTC	NP_001382101.1:n.414-382_414-381insTC
NM_001395173.1:c.414-382_414-381insTC	NP_001382102.1:n.414-382_414-381insTC
NM_001395174.1:c.414-382_414-381insTC	NP_001382103.1:n.414-382_414-381insTC
NM_001395175.1:c.411-382_411-381insTC	NP_001382104.1:n.411-382_411-381insTC