Canonical Allele Identifier: CA273914220

Gene: CHRNA3

Linked Data

• dbSNP Id: rs139280937
• gnomAD v3: 15-78615737-GTAT-G
• gnomAD v4: 15-78615737-GTAT-G
• MyVariant Identifiers: chr15:g.78908080_78908082del (hg19) ; chr15:g.78615738_78615740del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615739_78615741del , CM000677.2:g.78615739_78615741del	GRCh38
NC_000015.9:g.78908081_78908083del , CM000677.1:g.78908081_78908083del	GRCh37
NC_000015.8:g.76695136_76695138del	NCBI36
NG_016143.1:g.10556_10558del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1284_377+1286del MANE Select	ENSP00000315602.5:n.377+1284_377+1286del
ENST00000326828.5:c.377+1284_377+1286del	ENSP00000315602.5:n.377+1284_377+1286del
ENST00000348639.7:c.377+1284_377+1286del	ENSP00000267951.4:n.377+1284_377+1286del
ENST00000559658.5:c.377+1284_377+1286del	ENSP00000452896.1:n.377+1284_377+1286del
NM_000743.4:c.377+1284_377+1286del	NP_000734.2:n.377+1284_377+1286del
NM_001166694.1:c.377+1284_377+1286del	NP_001160166.1:n.377+1284_377+1286del
NR_046313.1:n.878+1284_878+1286del
XM_006720382.1:c.176+1284_176+1286del	XP_006720445.1:n.176+1284_176+1286del
XM_011521173.1:c.296+1284_296+1286del	XP_011519475.1:n.296+1284_296+1286del
XM_006720382.3:c.176+1284_176+1286del	XP_006720445.1:n.176+1284_176+1286del
NM_000743.5:c.377+1284_377+1286del MANE Select	NP_000734.2:n.377+1284_377+1286del
NM_001166694.2:c.377+1284_377+1286del	NP_001160166.1:n.377+1284_377+1286del
NR_046313.2:n.579+1284_579+1286del