Canonical Allele Identifier: CA2189601829

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615601_78615652delinsCAGACCCACTGACTCAGTGTTTCTGTGGGGCAGGACCTGGGGACAGGTATAG , CM000677.2:g.78615601_78615652delinsCAGACCCACTGACTCAGTGTTTCTGTGGGGCAGGACCTGGGGACAGGTATAG	GRCh38
NC_000015.9:g.78907943_78907994delinsCAGACCCACTGACTCAGTGTTTCTGTGGGGCAGGACCTGGGGACAGGTATAG , CM000677.1:g.78907943_78907994delinsCAGACCCACTGACTCAGTGTTTCTGTGGGGCAGGACCTGGGGACAGGTATAG	GRCh37
NC_000015.8:g.76694998_76695049delinsCAGACCCACTGACTCAGTGTTTCTGTGGGGCAGGACCTGGGGACAGGTATAG	NCBI36
NG_016143.1:g.10644_10695delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG MANE Select	ENSP00000315602.5:n.377+1372_377+1423deli...
ENST00000326828.5:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	ENSP00000315602.5:n.377+1372_377+1423deli...
ENST00000348639.7:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	ENSP00000267951.4:n.377+1372_377+1423deli...
ENST00000559658.5:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	ENSP00000452896.1:n.377+1372_377+1423deli...
NM_000743.4:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	NP_000734.2:n.377+1372_377+1423delinsCTAT...
NM_001166694.1:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	NP_001160166.1:n.377+1372_377+1423delinsC...
NR_046313.1:n.878+1372_878+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG
XM_006720382.1:c.176+1372_176+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	XP_006720445.1:n.176+1372_176+1423delinsC...
XM_011521173.1:c.296+1372_296+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	XP_011519475.1:n.296+1372_296+1423delinsC...
XM_006720382.3:c.176+1372_176+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	XP_006720445.1:n.176+1372_176+1423delinsC...
NM_000743.5:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG MANE Select	NP_000734.2:n.377+1372_377+1423delinsCTAT...
NM_001166694.2:c.377+1372_377+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG	NP_001160166.1:n.377+1372_377+1423delinsC...
NR_046313.2:n.579+1372_579+1423delinsCTATACCTGTCCCCAGGTCCTGCCCCACAGAAACACTGAGTCAGTGGGTCTG