Canonical Allele Identifier: CA2629788518

Gene: CHRNA5

Linked Data

• gnomAD v4: 15-78589428-A-AAAACGT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78589428_78589429insAAACGT , CM000677.2:g.78589428_78589429insAAACGT	GRCh38
NC_000015.9:g.78881770_78881771insAAACGT , CM000677.1:g.78881770_78881771insAAACGT	GRCh37
NC_000015.8:g.76668825_76668826insAAACGT	NCBI36
NG_023328.1:g.28909_28910insAAACGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.414-377_414-376insAAACGT MANE Select	ENSP00000299565.5:n.414-377_414-376insAAACGT
ENST00000394802.4:c.229-377_229-376insAAACGT
ENST00000559554.5:c.414-377_414-376insAAACGT	ENSP00000453519.1:n.414-377_414-376insAAACGT
NM_000745.3:c.414-377_414-376insAAACGT	NP_000736.2:n.414-377_414-376insAAACGT
NM_001307945.1:c.414-377_414-376insAAACGT	NP_001294874.1:n.414-377_414-376insAAACGT
XM_005254142.2:c.414-377_414-376insAAACGT	XP_005254199.1:n.414-377_414-376insAAACGT
NM_001307945.2:c.414-377_414-376insAAACGT	NP_001294874.1:n.414-377_414-376insAAACGT
NM_000745.4:c.414-377_414-376insAAACGT MANE Select	NP_000736.2:n.414-377_414-376insAAACGT
NM_001395171.1:c.414-377_414-376insAAACGT	NP_001382100.1:n.414-377_414-376insAAACGT
NM_001395172.1:c.414-377_414-376insAAACGT	NP_001382101.1:n.414-377_414-376insAAACGT
NM_001395173.1:c.414-377_414-376insAAACGT	NP_001382102.1:n.414-377_414-376insAAACGT
NM_001395174.1:c.414-377_414-376insAAACGT	NP_001382103.1:n.414-377_414-376insAAACGT
NM_001395175.1:c.411-377_411-376insAAACGT	NP_001382104.1:n.411-377_411-376insAAACGT