Canonical Allele Identifier: CA393589040

Gene: CHRNA3

Linked Data

• COSMIC: COSM6143036
• MyVariant Identifiers: chr15:g.78909405G>A (hg19) ; chr15:g.78617063G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617063G>A , CM000677.2:g.78617063G>A	GRCh38
NC_000015.9:g.78909405G>A , CM000677.1:g.78909405G>A	GRCh37
NC_000015.8:g.76696460G>A	NCBI36
NG_016143.1:g.9233C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.338C>T MANE Select	ENSP00000315602.5:p.Ala113Val
ENST00000326828.5:c.338C>T	ENSP00000315602.5:p.Ala113Val
ENST00000348639.7:c.338C>T	ENSP00000267951.4:p.Ala113Val
ENST00000559658.5:c.338C>T	ENSP00000452896.1:p.Ala113Val
NM_000743.4:c.338C>T	NP_000734.2:p.Ala113Val
NM_001166694.1:c.338C>T	NP_001160166.1:p.Ala113Val
NR_046313.1:n.839C>T
XM_006720382.1:c.137C>T	XP_006720445.1:p.Ala46Val
XM_011521173.1:c.257C>T	XP_011519475.1:p.Ala86Val
XM_006720382.3:c.137C>T	XP_006720445.1:p.Ala46Val
NM_000743.5:c.338C>T MANE Select	NP_000734.2:p.Ala113Val
NM_001166694.2:c.338C>T	NP_001160166.1:p.Ala113Val
NR_046313.2:n.540C>T