Canonical Allele Identifier: CA715973494

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1418653386
• gnomAD v3: 15-78615656-T-TA
• gnomAD v4: 15-78615656-T-TA
• MyVariant Identifiers: chr15:g.78907998_78907999insA (hg19) ; chr15:g.78615656_78615657insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615656_78615657insA , CM000677.2:g.78615656_78615657insA	GRCh38
NC_000015.9:g.78907998_78907999insA , CM000677.1:g.78907998_78907999insA	GRCh37
NC_000015.8:g.76695053_76695054insA	NCBI36
NG_016143.1:g.10639_10640insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1367_377+1368insT MANE Select	ENSP00000315602.5:n.377+1367_377+1368insT...
ENST00000326828.5:c.377+1367_377+1368insT	ENSP00000315602.5:n.377+1367_377+1368insT...
ENST00000348639.7:c.377+1367_377+1368insT	ENSP00000267951.4:n.377+1367_377+1368insT...
ENST00000559658.5:c.377+1367_377+1368insT	ENSP00000452896.1:n.377+1367_377+1368insT...
NM_000743.4:c.377+1367_377+1368insT	NP_000734.2:n.377+1367_377+1368insT
NM_001166694.1:c.377+1367_377+1368insT	NP_001160166.1:n.377+1367_377+1368insT
NR_046313.1:n.878+1367_878+1368insT
XM_006720382.1:c.176+1367_176+1368insT	XP_006720445.1:n.176+1367_176+1368insT
XM_011521173.1:c.296+1367_296+1368insT	XP_011519475.1:n.296+1367_296+1368insT
XM_006720382.3:c.176+1367_176+1368insT	XP_006720445.1:n.176+1367_176+1368insT
NM_000743.5:c.377+1367_377+1368insT MANE Select	NP_000734.2:n.377+1367_377+1368insT
NM_001166694.2:c.377+1367_377+1368insT	NP_001160166.1:n.377+1367_377+1368insT
NR_046313.2:n.579+1367_579+1368insT