Canonical Allele Identifier: CA619417556

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1442300685
• gnomAD v2: 15-78894627-C-CCATCATCA
• MyVariant Identifiers: chr15:g.78894627_78894628insCATCATCA (hg19) ; chr15:g.78602285_78602286insCATCATCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602285_78602286insCATCATCA , CM000677.2:g.78602285_78602286insCATCATCA	GRCh38
NC_000015.9:g.78894627_78894628insCATCATCA , CM000677.1:g.78894627_78894628insCATCATCA	GRCh37
NC_000015.8:g.76681682_76681683insCATCATCA	NCBI36
NG_016143.1:g.24010_24011insTGATGATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-22_378-21insTGATGATG MANE Select	ENSP00000315602.5:n.378-22_378-21insTGATGATG
ENST00000326828.5:c.378-22_378-21insTGATGATG	ENSP00000315602.5:n.378-22_378-21insTGATGATG
ENST00000348639.7:c.378-22_378-21insTGATGATG	ENSP00000267951.4:n.378-22_378-21insTGATGATG
ENST00000558903.1:n.85-22_85-21insTGATGATG
ENST00000559658.5:c.378-22_378-21insTGATGATG	ENSP00000452896.1:n.378-22_378-21insTGATGATG
NM_000743.4:c.378-22_378-21insTGATGATG	NP_000734.2:n.378-22_378-21insTGATGATG
NM_001166694.1:c.378-22_378-21insTGATGATG	NP_001160166.1:n.378-22_378-21insTGATGATG
NR_046313.1:n.879-22_879-21insTGATGATG
XM_006720382.1:c.177-22_177-21insTGATGATG	XP_006720445.1:n.177-22_177-21insTGATGATG
XM_011521173.1:c.297-22_297-21insTGATGATG	XP_011519475.1:n.297-22_297-21insTGATGATG
XM_006720382.3:c.177-22_177-21insTGATGATG	XP_006720445.1:n.177-22_177-21insTGATGATG
NM_000743.5:c.378-22_378-21insTGATGATG MANE Select	NP_000734.2:n.378-22_378-21insTGATGATG
NM_001166694.2:c.378-22_378-21insTGATGATG	NP_001160166.1:n.378-22_378-21insTGATGATG
NR_046313.2:n.580-22_580-21insTGATGATG