Canonical Allele Identifier: CA290079

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463498A>G , CM000670.2:g.27463498A>G	GRCh38
NC_000008.10:g.27321015A>G , CM000670.1:g.27321015A>G	GRCh37
NC_000008.9:g.27376932A>G	NCBI36
NG_015827.1:g.20799T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.945T>C MANE Select	ENSP00000385026.1:p.Thr315=
ENST00000637241.1:c.*775T>C	ENSP00000490690.1:n.*775T>C
ENST00000240132.7:c.900T>C	ENSP00000240132.2:p.Thr300=
ENST00000407991.2:c.945T>C	ENSP00000385026.1:p.Thr315=
ENST00000520600.1:n.290-1744T>C
ENST00000520933.7:c.879T>C	ENSP00000429616.2:p.Thr293=
ENST00000523695.5:c.*347T>C	ENSP00000430612.1:n.*347T>C
NM_000742.3:c.945T>C	NP_000733.2:p.Thr315=
NM_001282455.1:c.900T>C	NP_001269384.1:p.Thr300=
XM_005273397.1:c.468T>C	XP_005273454.1:p.Thr156=
XM_006716282.1:c.945T>C	XP_006716345.1:p.Thr315=
XM_011544388.1:c.945T>C	XP_011542690.1:p.Thr315=
XM_011544389.1:c.351T>C	XP_011542691.1:p.Thr117=
NM_001347705.1:c.468T>C	NP_001334634.1:p.Thr156=
NM_001347706.1:c.468T>C	NP_001334635.1:p.Thr156=
NM_001347707.1:c.351T>C	NP_001334636.1:p.Thr117=
NM_001347708.1:c.351T>C	NP_001334637.1:p.Thr117=
XM_011544389.2:c.351T>C	XP_011542691.1:p.Thr117=
NM_000742.4:c.945T>C MANE Select	NP_000733.2:p.Thr315=
NM_001282455.2:c.900T>C	NP_001269384.1:p.Thr300=
NM_001347705.2:c.468T>C	NP_001334634.1:p.Thr156=
NM_001347706.2:c.468T>C	NP_001334635.1:p.Thr156=
NM_001347707.2:c.351T>C	NP_001334636.1:p.Thr117=
NM_001347708.2:c.351T>C	NP_001334637.1:p.Thr117=