Canonical Allele Identifier: CA393576209

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78618844-G-A
• COSMIC: COSM3887551
• MyVariant Identifiers: chr15:g.78911186G>A (hg19) ; chr15:g.78618844G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618844G>A , CM000677.2:g.78618844G>A	GRCh38
NC_000015.9:g.78911186G>A , CM000677.1:g.78911186G>A	GRCh37
NC_000015.8:g.76698241G>A	NCBI36
NG_016143.1:g.7452C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.154C>T MANE Select	ENSP00000315602.5:p.Pro52Ser
ENST00000326828.5:c.154C>T	ENSP00000315602.5:p.Pro52Ser
ENST00000348639.7:c.154C>T	ENSP00000267951.4:p.Pro52Ser
ENST00000559080.1:c.-48C>T	ENSP00000453993.1:n.-48C>T
ENST00000559658.5:c.154C>T	ENSP00000452896.1:p.Pro52Ser
ENST00000561128.1:n.149C>T
NM_000743.4:c.154C>T	NP_000734.2:p.Pro52Ser
NM_001166694.1:c.154C>T	NP_001160166.1:p.Pro52Ser
NR_046313.1:n.655C>T
XM_006720382.1:c.-48C>T	XP_006720445.1:n.-48C>T
XM_011521173.1:c.73C>T	XP_011519475.1:p.Pro25Ser
XM_006720382.3:c.-48C>T	XP_006720445.1:n.-48C>T
NM_000743.5:c.154C>T MANE Select	NP_000734.2:p.Pro52Ser
NM_001166694.2:c.154C>T	NP_001160166.1:p.Pro52Ser
NR_046313.2:n.356C>T