Canonical Allele Identifier: CA393584712

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894181T>G (hg19) ; chr15:g.78601839T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601839T>G , CM000677.2:g.78601839T>G	GRCh38
NC_000015.9:g.78894181T>G , CM000677.1:g.78894181T>G	GRCh37
NC_000015.8:g.76681236T>G	NCBI36
NG_016143.1:g.24457A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.803A>C MANE Select	ENSP00000315602.5:p.Asp268Ala
ENST00000326828.5:c.803A>C	ENSP00000315602.5:p.Asp268Ala
ENST00000348639.7:c.803A>C	ENSP00000267951.4:p.Asp268Ala
ENST00000558903.1:n.510A>C
ENST00000559658.5:c.803A>C	ENSP00000452896.1:p.Asp268Ala
NM_000743.4:c.803A>C	NP_000734.2:p.Asp268Ala
NM_001166694.1:c.803A>C	NP_001160166.1:p.Asp268Ala
NR_046313.1:n.1304A>C
XM_006720382.1:c.602A>C	XP_006720445.1:p.Asp201Ala
XM_011521173.1:c.722A>C	XP_011519475.1:p.Asp241Ala
XM_006720382.3:c.602A>C	XP_006720445.1:p.Asp201Ala
NM_000743.5:c.803A>C MANE Select	NP_000734.2:p.Asp268Ala
NM_001166694.2:c.803A>C	NP_001160166.1:p.Asp268Ala
NR_046313.2:n.1005A>C