Canonical Allele Identifier: CA2580090049

Gene: CHRNA3

Linked Data

• ClinVar Variation Id: 2431100
• ClinVar RCV Id: RCV003129633

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602493_78602494delinsTG , CM000677.2:g.78602493_78602494delinsTG	GRCh38
NC_000015.9:g.78894835_78894836delinsTG , CM000677.1:g.78894835_78894836delinsTG	GRCh37
NC_000015.8:g.76681890_76681891delinsTG	NCBI36
NG_016143.1:g.23802_23803delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.378-230_378-229delinsCA MANE Select	ENSP00000315602.5:n.378-230_378-229delinsCA
ENST00000326828.5:c.378-230_378-229delinsCA	ENSP00000315602.5:n.378-230_378-229delinsCA
ENST00000348639.7:c.378-230_378-229delinsCA	ENSP00000267951.4:n.378-230_378-229delinsCA
ENST00000558903.1:n.85-230_85-229delinsCA
ENST00000559658.5:c.378-230_378-229delinsCA	ENSP00000452896.1:n.378-230_378-229delinsCA
NM_000743.4:c.378-230_378-229delinsCA	NP_000734.2:n.378-230_378-229delinsCA
NM_001166694.1:c.378-230_378-229delinsCA	NP_001160166.1:n.378-230_378-229delinsCA
NR_046313.1:n.879-230_879-229delinsCA
XM_006720382.1:c.177-230_177-229delinsCA	XP_006720445.1:n.177-230_177-229delinsCA
XM_011521173.1:c.297-230_297-229delinsCA	XP_011519475.1:n.297-230_297-229delinsCA
XM_006720382.3:c.177-230_177-229delinsCA	XP_006720445.1:n.177-230_177-229delinsCA
NM_000743.5:c.378-230_378-229delinsCA MANE Select	NP_000734.2:n.378-230_378-229delinsCA
NM_001166694.2:c.378-230_378-229delinsCA	NP_001160166.1:n.378-230_378-229delinsCA
NR_046313.2:n.580-230_580-229delinsCA