Canonical Allele Identifier: CA1772813812

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463290_27463291delinsGT , CM000670.2:g.27463290_27463291delinsGT	GRCh38
NC_000008.10:g.27320807_27320808delinsGT , CM000670.1:g.27320807_27320808delinsGT	GRCh37
NC_000008.9:g.27376724_27376725delinsGT	NCBI36
NG_015827.1:g.21006_21007delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1152_1153delinsAC MANE Select	ENSP00000385026.1:p.Pro384=
ENST00000240132.7:c.1107_1108delinsAC	ENSP00000240132.2:p.Pro369=
ENST00000407991.2:c.1152_1153delinsAC	ENSP00000385026.1:p.Pro384=
ENST00000520600.1:n.290-1537_290-1536delinsAC
ENST00000520933.7:c.1086_1087delinsAC	ENSP00000429616.2:p.Pro362=
ENST00000523695.5:c.*554_*555delinsAC	ENSP00000430612.1:n.*554_*555delinsAC
NM_000742.3:c.1152_1153delinsAC	NP_000733.2:p.Pro384=
NM_001282455.1:c.1107_1108delinsAC	NP_001269384.1:p.Pro369=
XM_005273397.1:c.675_676delinsAC	XP_005273454.1:p.Pro225=
XM_006716282.1:c.1152_1153delinsAC	XP_006716345.1:p.Pro384=
XM_011544388.1:c.1152_1153delinsAC	XP_011542690.1:p.Pro384=
XM_011544389.1:c.558_559delinsAC	XP_011542691.1:p.Pro186=
NM_001347705.1:c.675_676delinsAC	NP_001334634.1:p.Pro225=
NM_001347706.1:c.675_676delinsAC	NP_001334635.1:p.Pro225=
NM_001347707.1:c.558_559delinsAC	NP_001334636.1:p.Pro186=
NM_001347708.1:c.558_559delinsAC	NP_001334637.1:p.Pro186=
XM_011544389.2:c.558_559delinsAC	XP_011542691.1:p.Pro186=
NM_000742.4:c.1152_1153delinsAC MANE Select	NP_000733.2:p.Pro384=
NM_001282455.2:c.1107_1108delinsAC	NP_001269384.1:p.Pro369=
NM_001347705.2:c.675_676delinsAC	NP_001334634.1:p.Pro225=
NM_001347706.2:c.675_676delinsAC	NP_001334635.1:p.Pro225=
NM_001347707.2:c.558_559delinsAC	NP_001334636.1:p.Pro186=
NM_001347708.2:c.558_559delinsAC	NP_001334637.1:p.Pro186=