Canonical Allele Identifier: CA2189599079

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053100885

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595957_78595959dup , CM000677.2:g.78595957_78595959dup	GRCh38
NC_000015.9:g.78888299_78888301dup , CM000677.1:g.78888299_78888301dup	GRCh37
NC_000015.8:g.76675354_76675356dup	NCBI36
NG_016143.1:g.30338_30340dup
NG_023328.1:g.35438_35440dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*646_*648dup MANE Select	ENSP00000315602.5:n.*646_*648dup
ENST00000326828.5:c.*646_*648dup	ENSP00000315602.5:n.*646_*648dup
ENST00000348639.7:c.1390-2767_1390-2765dup	ENSP00000267951.4:n.1390-2767_1390-2765du...
ENST00000559002.5:n.193+582_193+584dup
ENST00000559658.5:c.*64+582_*64+584dup	ENSP00000452896.1:n.*64+582_*64+584dup
NM_000743.4:c.*646_*648dup	NP_000734.2:n.*646_*648dup
NM_001166694.1:c.1390-2767_1390-2765dup	NP_001160166.1:n.1390-2767_1390-2765dup
NR_046313.1:n.2083+582_2083+584dup
XM_006720382.1:c.*646_*648dup	XP_006720445.1:n.*646_*648dup
XM_011521173.1:c.*646_*648dup	XP_011519475.1:n.*646_*648dup
XM_006720382.3:c.*646_*648dup	XP_006720445.1:n.*646_*648dup
NM_000743.5:c.*646_*648dup MANE Select	NP_000734.2:n.*646_*648dup
NM_001166694.2:c.1390-2767_1390-2765dup	NP_001160166.1:n.1390-2767_1390-2765dup
NR_046313.2:n.1784+582_1784+584dup