Canonical Allele Identifier: CA619234984

Gene: CHRNA3

Linked Data

• dbSNP Id: rs10637216
• gnomAD v2: 15-78888234-A-ACCCCC
• gnomAD v3: 15-78595892-A-ACCCCC
• gnomAD v4: 15-78595892-A-ACCCCC
• MyVariant Identifiers: chr15:g.78888234_78888235insCCCCC (hg19) ; chr15:g.78595892_78595893insCCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595895_78595896insCCCCC , CM000677.2:g.78595895_78595896insCCCCC	GRCh38
NC_000015.9:g.78888237_78888238insCCCCC , CM000677.1:g.78888237_78888238insCCCCC	GRCh37
NC_000015.8:g.76675292_76675293insCCCCC	NCBI36
NG_016143.1:g.30403_30404insGGGGG
NG_023328.1:g.35376_35377insCCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*711_*712insGGGGG MANE Select	ENSP00000315602.5:n.*711_*712insGGGGG
ENST00000326828.5:c.*711_*712insGGGGG	ENSP00000315602.5:n.*711_*712insGGGGG
ENST00000348639.7:c.1390-2702_1390-2701insGGGGG	ENSP00000267951.4:n.1390-2702_1390-2701insGGGGG
ENST00000559002.5:n.193+647_193+648insGGGGG
ENST00000559658.5:c.*64+647_*64+648insGGGGG	ENSP00000452896.1:n.*64+647_*64+648insGGGGG
NM_000743.4:c.*711_*712insGGGGG	NP_000734.2:n.*711_*712insGGGGG
NM_001166694.1:c.1390-2702_1390-2701insGGGGG	NP_001160166.1:n.1390-2702_1390-2701insGGGGG
NR_046313.1:n.2083+647_2083+648insGGGGG
XM_006720382.1:c.*711_*712insGGGGG	XP_006720445.1:n.*711_*712insGGGGG
XM_011521173.1:c.*711_*712insGGGGG	XP_011519475.1:n.*711_*712insGGGGG
XM_006720382.3:c.*711_*712insGGGGG	XP_006720445.1:n.*711_*712insGGGGG
NM_000743.5:c.*711_*712insGGGGG MANE Select	NP_000734.2:n.*711_*712insGGGGG
NM_001166694.2:c.1390-2702_1390-2701insGGGGG	NP_001160166.1:n.1390-2702_1390-2701insGGGGG
NR_046313.2:n.1784+647_1784+648insGGGGG