Canonical Allele Identifier: CA919597478

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1596083308

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615709_78615711del , CM000677.2:g.78615709_78615711del	GRCh38
NC_000015.9:g.78908051_78908053del , CM000677.1:g.78908051_78908053del	GRCh37
NC_000015.8:g.76695106_76695108del	NCBI36
NG_016143.1:g.10587_10589del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1315_377+1317del MANE Select	ENSP00000315602.5:n.377+1315_377+1317del
ENST00000326828.5:c.377+1315_377+1317del	ENSP00000315602.5:n.377+1315_377+1317del
ENST00000348639.7:c.377+1315_377+1317del	ENSP00000267951.4:n.377+1315_377+1317del
ENST00000559658.5:c.377+1315_377+1317del	ENSP00000452896.1:n.377+1315_377+1317del
NM_000743.4:c.377+1315_377+1317del	NP_000734.2:n.377+1315_377+1317del
NM_001166694.1:c.377+1315_377+1317del	NP_001160166.1:n.377+1315_377+1317del
NR_046313.1:n.878+1315_878+1317del
XM_006720382.1:c.176+1315_176+1317del	XP_006720445.1:n.176+1315_176+1317del
XM_011521173.1:c.296+1315_296+1317del	XP_011519475.1:n.296+1315_296+1317del
XM_006720382.3:c.176+1315_176+1317del	XP_006720445.1:n.176+1315_176+1317del
NM_000743.5:c.377+1315_377+1317del MANE Select	NP_000734.2:n.377+1315_377+1317del
NM_001166694.2:c.377+1315_377+1317del	NP_001160166.1:n.377+1315_377+1317del
NR_046313.2:n.579+1315_579+1317del