Canonical Allele Identifier: CA2686678225
Gene: CHRNA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27463320_27463321dup , CM000670.2:g.27463320_27463321dup GRCh38
NC_000008.10:g.27320837_27320838dup , CM000670.1:g.27320837_27320838dup GRCh37
NC_000008.9:g.27376754_27376755dup NCBI36
NG_015827.1:g.20976_20977dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000407991.3:c.1122_1123dup MANE Select ENSP00000385026.1:p.Pro375ArgfsTer6
ENST00000240132.7:c.1077_1078dup ENSP00000240132.2:p.Pro360ArgfsTer6
ENST00000407991.2:c.1122_1123dup ENSP00000385026.1:p.Pro375ArgfsTer6
ENST00000520600.1:n.290-1567_290-1566dup
ENST00000520933.7:c.1056_1057dup ENSP00000429616.2:p.Pro353ArgfsTer6
ENST00000523695.5:c.*524_*525dup ENSP00000430612.1:n.*524_*525dup
NM_000742.3:c.1122_1123dup NP_000733.2:p.Pro375ArgfsTer6
NM_001282455.1:c.1077_1078dup NP_001269384.1:p.Pro360ArgfsTer6
XM_005273397.1:c.645_646dup XP_005273454.1:p.Pro216ArgfsTer6
XM_006716282.1:c.1122_1123dup XP_006716345.1:p.Pro375ArgfsTer6
XM_011544388.1:c.1122_1123dup XP_011542690.1:p.Pro375ArgfsTer6
XM_011544389.1:c.528_529dup XP_011542691.1:p.Pro177ArgfsTer6
NM_001347705.1:c.645_646dup NP_001334634.1:p.Pro216ArgfsTer6
NM_001347706.1:c.645_646dup NP_001334635.1:p.Pro216ArgfsTer6
NM_001347707.1:c.528_529dup NP_001334636.1:p.Pro177ArgfsTer6
NM_001347708.1:c.528_529dup NP_001334637.1:p.Pro177ArgfsTer6
XM_011544389.2:c.528_529dup XP_011542691.1:p.Pro177ArgfsTer6
NM_000742.4:c.1122_1123dup MANE Select NP_000733.2:p.Pro375ArgfsTer6
NM_001282455.2:c.1077_1078dup NP_001269384.1:p.Pro360ArgfsTer6
NM_001347705.2:c.645_646dup NP_001334634.1:p.Pro216ArgfsTer6
NM_001347706.2:c.645_646dup NP_001334635.1:p.Pro216ArgfsTer6
NM_001347707.2:c.528_529dup NP_001334636.1:p.Pro177ArgfsTer6
NM_001347708.2:c.528_529dup NP_001334637.1:p.Pro177ArgfsTer6