Canonical Allele Identifier: CA971789313

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053450459
• gnomAD v3: 15-78615695-CAGTG-C
• gnomAD v4: 15-78615695-CAGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615698_78615701del , CM000677.2:g.78615698_78615701del	GRCh38
NC_000015.9:g.78908040_78908043del , CM000677.1:g.78908040_78908043del	GRCh37
NC_000015.8:g.76695095_76695098del	NCBI36
NG_016143.1:g.10597_10600del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1325_377+1328del MANE Select	ENSP00000315602.5:n.377+1325_377+1328del
ENST00000326828.5:c.377+1325_377+1328del	ENSP00000315602.5:n.377+1325_377+1328del
ENST00000348639.7:c.377+1325_377+1328del	ENSP00000267951.4:n.377+1325_377+1328del
ENST00000559658.5:c.377+1325_377+1328del	ENSP00000452896.1:n.377+1325_377+1328del
NM_000743.4:c.377+1325_377+1328del	NP_000734.2:n.377+1325_377+1328del
NM_001166694.1:c.377+1325_377+1328del	NP_001160166.1:n.377+1325_377+1328del
NR_046313.1:n.878+1325_878+1328del
XM_006720382.1:c.176+1325_176+1328del	XP_006720445.1:n.176+1325_176+1328del
XM_011521173.1:c.296+1325_296+1328del	XP_011519475.1:n.296+1325_296+1328del
XM_006720382.3:c.176+1325_176+1328del	XP_006720445.1:n.176+1325_176+1328del
NM_000743.5:c.377+1325_377+1328del MANE Select	NP_000734.2:n.377+1325_377+1328del
NM_001166694.2:c.377+1325_377+1328del	NP_001160166.1:n.377+1325_377+1328del
NR_046313.2:n.579+1325_579+1328del