Canonical Allele Identifier: CA971789331

Gene: CHRNA3

Linked Data

• gnomAD v3: 15-78615739-A-ATTTTTT
• gnomAD v4: 15-78615739-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615756_78615761dup , CM000677.2:g.78615756_78615761dup	GRCh38
NC_000015.9:g.78908098_78908103dup , CM000677.1:g.78908098_78908103dup	GRCh37
NC_000015.8:g.76695153_76695158dup	NCBI36
NG_016143.1:g.10551_10556dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.377+1279_377+1284dup MANE Select	ENSP00000315602.5:n.377+1279_377+1284dup
ENST00000326828.5:c.377+1279_377+1284dup	ENSP00000315602.5:n.377+1279_377+1284dup
ENST00000348639.7:c.377+1279_377+1284dup	ENSP00000267951.4:n.377+1279_377+1284dup
ENST00000559658.5:c.377+1279_377+1284dup	ENSP00000452896.1:n.377+1279_377+1284dup
NM_000743.4:c.377+1279_377+1284dup	NP_000734.2:n.377+1279_377+1284dup
NM_001166694.1:c.377+1279_377+1284dup	NP_001160166.1:n.377+1279_377+1284dup
NR_046313.1:n.878+1279_878+1284dup
XM_006720382.1:c.176+1279_176+1284dup	XP_006720445.1:n.176+1279_176+1284dup
XM_011521173.1:c.296+1279_296+1284dup	XP_011519475.1:n.296+1279_296+1284dup
XM_006720382.3:c.176+1279_176+1284dup	XP_006720445.1:n.176+1279_176+1284dup
NM_000743.5:c.377+1279_377+1284dup MANE Select	NP_000734.2:n.377+1279_377+1284dup
NM_001166694.2:c.377+1279_377+1284dup	NP_001160166.1:n.377+1279_377+1284dup
NR_046313.2:n.579+1279_579+1284dup