Canonical Allele Identifier: CA619238138

Gene: CHRNA3

Linked Data

• dbSNP Id: rs532401932
• gnomAD v2: 15-78908081-ATT-A
• gnomAD v3: 15-78615739-ATT-A
• gnomAD v4: 15-78615739-ATT-A
• MyVariant Identifiers: chr15:g.78908084_78908085del (hg19) ; chr15:g.78908082_78908083del (hg19) ; chr15:g.78615742_78615743del (hg38) ; chr15:g.78615740_78615741del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615760_78615761del , CM000677.2:g.78615760_78615761del	GRCh38
NC_000015.9:g.78908102_78908103del , CM000677.1:g.78908102_78908103del	GRCh37
NC_000015.8:g.76695157_76695158del	NCBI36
NG_016143.1:g.10555_10556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.377+1283_377+1284del MANE Select	ENSP00000315602.5:n.377+1283_377+1284del
ENST00000326828.5:c.377+1283_377+1284del	ENSP00000315602.5:n.377+1283_377+1284del
ENST00000348639.7:c.377+1283_377+1284del	ENSP00000267951.4:n.377+1283_377+1284del
ENST00000559658.5:c.377+1283_377+1284del	ENSP00000452896.1:n.377+1283_377+1284del
NM_000743.4:c.377+1283_377+1284del	NP_000734.2:n.377+1283_377+1284del
NM_001166694.1:c.377+1283_377+1284del	NP_001160166.1:n.377+1283_377+1284del
NR_046313.1:n.878+1283_878+1284del
XM_006720382.1:c.176+1283_176+1284del	XP_006720445.1:n.176+1283_176+1284del
XM_011521173.1:c.296+1283_296+1284del	XP_011519475.1:n.296+1283_296+1284del
XM_006720382.3:c.176+1283_176+1284del	XP_006720445.1:n.176+1283_176+1284del
NM_000743.5:c.377+1283_377+1284del MANE Select	NP_000734.2:n.377+1283_377+1284del
NM_001166694.2:c.377+1283_377+1284del	NP_001160166.1:n.377+1283_377+1284del
NR_046313.2:n.579+1283_579+1284del