Canonical Allele Identifier: CA715961338

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1358770507
• gnomAD v3: 15-78599398-CTACTT-C
• gnomAD v4: 15-78599398-CTACTT-C
• MyVariant Identifiers: chr15:g.78891741_78891745del (hg19) ; chr15:g.78599399_78599403del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78599401_78599405del , CM000677.2:g.78599401_78599405del	GRCh38
NC_000015.9:g.78891743_78891747del , CM000677.1:g.78891743_78891747del	GRCh37
NC_000015.8:g.76678798_76678802del	NCBI36
NG_016143.1:g.26893_26897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.1389+1850_1389+1854del MANE Select	ENSP00000315602.5:n.1389+1850_1389+1854del
ENST00000326828.5:c.1389+1850_1389+1854del	ENSP00000315602.5:n.1389+1850_1389+1854del
ENST00000348639.7:c.1389+1850_1389+1854del	ENSP00000267951.4:n.1389+1850_1389+1854del
ENST00000559658.5:c.1389+1850_1389+1854del	ENSP00000452896.1:n.1389+1850_1389+1854del
NM_000743.4:c.1389+1850_1389+1854del	NP_000734.2:n.1389+1850_1389+1854del
NM_001166694.1:c.1389+1850_1389+1854del	NP_001160166.1:n.1389+1850_1389+1854del
NR_046313.1:n.1890+1850_1890+1854del
XM_006720382.1:c.1188+1850_1188+1854del	XP_006720445.1:n.1188+1850_1188+1854del
XM_011521173.1:c.1308+1850_1308+1854del	XP_011519475.1:n.1308+1850_1308+1854del
XM_006720382.3:c.1188+1850_1188+1854del	XP_006720445.1:n.1188+1850_1188+1854del
NM_000743.5:c.1389+1850_1389+1854del MANE Select	NP_000734.2:n.1389+1850_1389+1854del
NM_001166694.2:c.1389+1850_1389+1854del	NP_001160166.1:n.1389+1850_1389+1854del
NR_046313.2:n.1591+1850_1591+1854del