Canonical Allele Identifier: CA645550781

Gene: CHRNA2

Linked Data

• COSMIC: COSM5446459

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463183del , CM000670.2:g.27463183del	GRCh38
NC_000008.10:g.27320700del , CM000670.1:g.27320700del	GRCh37
NC_000008.9:g.27376617del	NCBI36
NG_015827.1:g.21115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1261del MANE Select	ENSP00000385026.1:p.Asp421ThrfsTer?
ENST00000240132.7:c.1216del	ENSP00000240132.2:p.Asp406ThrfsTer?
ENST00000407991.2:c.1261del	ENSP00000385026.1:p.Asp421ThrfsTer?
ENST00000520600.1:n.290-1428del
ENST00000520933.7:c.1195del	ENSP00000429616.2:p.Asp399ThrfsTer?
ENST00000523695.5:c.*663del	ENSP00000430612.1:n.*663del
NM_000742.3:c.1261del	NP_000733.2:p.Asp421ThrfsTer?
NM_001282455.1:c.1216del	NP_001269384.1:p.Asp406ThrfsTer?
XM_005273397.1:c.784del	XP_005273454.1:p.Asp262ThrfsTer?
XM_006716282.1:c.1261del	XP_006716345.1:p.Asp421ThrfsTer?
XM_011544388.1:c.1261del	XP_011542690.1:p.Asp421ThrfsTer?
XM_011544389.1:c.667del	XP_011542691.1:p.Asp223ThrfsTer?
NM_001347705.1:c.784del	NP_001334634.1:p.Asp262ThrfsTer?
NM_001347706.1:c.784del	NP_001334635.1:p.Asp262ThrfsTer?
NM_001347707.1:c.667del	NP_001334636.1:p.Asp223ThrfsTer?
NM_001347708.1:c.667del	NP_001334637.1:p.Asp223ThrfsTer?
XM_011544389.2:c.667del	XP_011542691.1:p.Asp223ThrfsTer?
NM_000742.4:c.1261del MANE Select	NP_000733.2:p.Asp421ThrfsTer?
NM_001282455.2:c.1216del	NP_001269384.1:p.Asp406ThrfsTer?
NM_001347705.2:c.784del	NP_001334634.1:p.Asp262ThrfsTer?
NM_001347706.2:c.784del	NP_001334635.1:p.Asp262ThrfsTer?
NM_001347707.2:c.667del	NP_001334636.1:p.Asp223ThrfsTer?
NM_001347708.2:c.667del	NP_001334637.1:p.Asp223ThrfsTer?