Canonical Allele Identifier: CA619417593

Gene: CHRNA5

Linked Data

• dbSNP Id: rs1424525018
• gnomAD v2: 15-78881763-AG-A
• gnomAD v3: 15-78589421-AG-A
• gnomAD v4: 15-78589421-AG-A
• MyVariant Identifiers: chr15:g.78881764del (hg19) ; chr15:g.78589422del (hg38)

Genomic Alleles

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

Transcript Alleles

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