Canonical Allele Identifier: CA971779378

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053099472
• gnomAD v3: 15-78595893-C-CCCCG
• gnomAD v4: 15-78595893-C-CCCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595895_78595896insCGCC , CM000677.2:g.78595895_78595896insCGCC	GRCh38
NC_000015.9:g.78888237_78888238insCGCC , CM000677.1:g.78888237_78888238insCGCC	GRCh37
NC_000015.8:g.76675292_76675293insCGCC	NCBI36
NG_016143.1:g.30402_30403insCGGG
NG_023328.1:g.35376_35377insCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*710_*711insCGGG MANE Select	ENSP00000315602.5:n.*710_*711insCGGG
ENST00000326828.5:c.*710_*711insCGGG	ENSP00000315602.5:n.*710_*711insCGGG
ENST00000348639.7:c.1390-2703_1390-2702insCGGG	ENSP00000267951.4:n.1390-2703_1390-2702insCGGG
ENST00000559002.5:n.193+646_193+647insCGGG
ENST00000559658.5:c.*64+646_*64+647insCGGG	ENSP00000452896.1:n.*64+646_*64+647insCGGG
NM_000743.4:c.*710_*711insCGGG	NP_000734.2:n.*710_*711insCGGG
NM_001166694.1:c.1390-2703_1390-2702insCGGG	NP_001160166.1:n.1390-2703_1390-2702insCGGG
NR_046313.1:n.2083+646_2083+647insCGGG
XM_006720382.1:c.*710_*711insCGGG	XP_006720445.1:n.*710_*711insCGGG
XM_011521173.1:c.*710_*711insCGGG	XP_011519475.1:n.*710_*711insCGGG
XM_006720382.3:c.*710_*711insCGGG	XP_006720445.1:n.*710_*711insCGGG
NM_000743.5:c.*710_*711insCGGG MANE Select	NP_000734.2:n.*710_*711insCGGG
NM_001166694.2:c.1390-2703_1390-2702insCGGG	NP_001160166.1:n.1390-2703_1390-2702insCGGG
NR_046313.2:n.1784+646_1784+647insCGGG