Canonical Allele Identifier: CA12877548
Gene: CHRNA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27472579C>T , CM000670.2:g.27472579C>T GRCh38
NC_000008.10:g.27330096C>T , CM000670.1:g.27330096C>T GRCh37
NC_000008.9:g.27386013C>T NCBI36
NG_015827.1:g.11718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407991.3:c.-136-1385G>A MANE Select ENSP00000385026.1:n.-136-1385G>A
ENST00000637241.1:c.-136-1385G>A ENSP00000490690.1:n.-136-1385G>A
ENST00000637361.1:n.95-1385G>A
ENST00000240132.7:c.-136-1385G>A ENSP00000240132.2:n.-136-1385G>A
ENST00000407991.2:c.-136-1385G>A ENSP00000385026.1:n.-136-1385G>A
ENST00000518712.5:c.-136-1385G>A ENSP00000430856.1:n.-136-1385G>A
ENST00000520208.1:c.-136-1385G>A ENSP00000430994.1:n.-136-1385G>A
ENST00000520650.2:n.469-1346G>A
ENST00000520933.7:c.-252-1385G>A ENSP00000429616.2:n.-252-1385G>A
ENST00000521921.5:c.-136-1385G>A ENSP00000429953.1:n.-136-1385G>A
ENST00000523695.5:c.-136-1385G>A ENSP00000430612.1:n.-136-1385G>A
ENST00000524096.5:c.-136-1385G>A ENSP00000430422.1:n.-136-1385G>A
NM_000742.3:c.-136-1385G>A NP_000733.2:n.-136-1385G>A
NM_001282455.1:c.-136-1385G>A NP_001269384.1:n.-136-1385G>A
XM_006716282.1:c.-136-1385G>A XP_006716345.1:n.-136-1385G>A
XM_011544388.1:c.-136-1385G>A XP_011542690.1:n.-136-1385G>A
XM_011544389.1:c.-594-1385G>A XP_011542691.1:n.-594-1385G>A
NM_001347705.1:c.-563-1385G>A NP_001334634.1:n.-563-1385G>A
NM_001347706.1:c.-608-1385G>A NP_001334635.1:n.-608-1385G>A
NM_001347707.1:c.-549-1385G>A NP_001334636.1:n.-549-1385G>A
NM_001347708.1:c.-597-1385G>A NP_001334637.1:n.-597-1385G>A
XM_011544389.2:c.-594-1385G>A XP_011542691.1:n.-594-1385G>A
NM_000742.4:c.-136-1385G>A MANE Select NP_000733.2:n.-136-1385G>A
NM_001282455.2:c.-136-1385G>A NP_001269384.1:n.-136-1385G>A
NM_001347705.2:c.-563-1385G>A NP_001334634.1:n.-563-1385G>A
NM_001347706.2:c.-608-1385G>A NP_001334635.1:n.-608-1385G>A
NM_001347707.2:c.-549-1385G>A NP_001334636.1:n.-549-1385G>A
NM_001347708.2:c.-597-1385G>A NP_001334637.1:n.-597-1385G>A
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