Canonical Allele Identifier: CA645550782
Gene: CHRNA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27463204_27463205delinsTT , CM000670.2:g.27463204_27463205delinsTT GRCh38
NC_000008.10:g.27320721_27320722delinsTT , CM000670.1:g.27320721_27320722delinsTT GRCh37
NC_000008.9:g.27376638_27376639delinsTT NCBI36
NG_015827.1:g.21092_21093delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000407991.3:c.1238_1239delinsAA MANE Select ENSP00000385026.1:p.Arg413Lys
ENST00000240132.7:c.1193_1194delinsAA ENSP00000240132.2:p.Arg398Lys
ENST00000407991.2:c.1238_1239delinsAA ENSP00000385026.1:p.Arg413Lys
ENST00000520600.1:n.290-1451_290-1450delinsAA
ENST00000520933.7:c.1172_1173delinsAA ENSP00000429616.2:p.Arg391Lys
ENST00000523695.5:c.*640_*641delinsAA ENSP00000430612.1:n.*640_*641delinsAA
NM_000742.3:c.1238_1239delinsAA NP_000733.2:p.Arg413Lys
NM_001282455.1:c.1193_1194delinsAA NP_001269384.1:p.Arg398Lys
XM_005273397.1:c.761_762delinsAA XP_005273454.1:p.Arg254Lys
XM_006716282.1:c.1238_1239delinsAA XP_006716345.1:p.Arg413Lys
XM_011544388.1:c.1238_1239delinsAA XP_011542690.1:p.Arg413Lys
XM_011544389.1:c.644_645delinsAA XP_011542691.1:p.Arg215Lys
NM_001347705.1:c.761_762delinsAA NP_001334634.1:p.Arg254Lys
NM_001347706.1:c.761_762delinsAA NP_001334635.1:p.Arg254Lys
NM_001347707.1:c.644_645delinsAA NP_001334636.1:p.Arg215Lys
NM_001347708.1:c.644_645delinsAA NP_001334637.1:p.Arg215Lys
XM_011544389.2:c.644_645delinsAA XP_011542691.1:p.Arg215Lys
NM_000742.4:c.1238_1239delinsAA MANE Select NP_000733.2:p.Arg413Lys
NM_001282455.2:c.1193_1194delinsAA NP_001269384.1:p.Arg398Lys
NM_001347705.2:c.761_762delinsAA NP_001334634.1:p.Arg254Lys
NM_001347706.2:c.761_762delinsAA NP_001334635.1:p.Arg254Lys
NM_001347707.2:c.644_645delinsAA NP_001334636.1:p.Arg215Lys
NM_001347708.2:c.644_645delinsAA NP_001334637.1:p.Arg215Lys