Canonical Allele Identifier: CA370813726

Gene: CHRNA2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27470995T>A , CM000670.2:g.27470995T>A	GRCh38
NC_000008.10:g.27328512T>A , CM000670.1:g.27328512T>A	GRCh37
NC_000008.9:g.27384429T>A	NCBI36
NG_015827.1:g.13302A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.64A>T MANE Select	ENSP00000385026.1:p.Thr22Ser
ENST00000637241.1:c.64A>T	ENSP00000490690.1:p.Thr22Ser
ENST00000240132.7:c.64A>T	ENSP00000240132.2:p.Thr22Ser
ENST00000407991.2:c.64A>T	ENSP00000385026.1:p.Thr22Ser
ENST00000518712.5:c.64A>T	ENSP00000430856.1:p.Thr22Ser
ENST00000520933.7:c.-53A>T	ENSP00000429616.2:n.-53A>T
ENST00000521921.5:c.64A>T	ENSP00000429953.1:p.Thr22Ser
ENST00000523695.5:c.64A>T	ENSP00000430612.1:p.Thr22Ser
ENST00000524096.5:c.64A>T	ENSP00000430422.1:p.Thr22Ser
NM_000742.3:c.64A>T	NP_000733.2:p.Thr22Ser
NM_001282455.1:c.64A>T	NP_001269384.1:p.Thr22Ser
XM_006716282.1:c.64A>T	XP_006716345.1:p.Thr22Ser
XM_011544388.1:c.64A>T	XP_011542690.1:p.Thr22Ser
XM_011544389.1:c.-395A>T	XP_011542691.1:n.-395A>T
NM_001347705.1:c.-364A>T	NP_001334634.1:n.-364A>T
NM_001347706.1:c.-409A>T	NP_001334635.1:n.-409A>T
NM_001347707.1:c.-350A>T	NP_001334636.1:n.-350A>T
NM_001347708.1:c.-398A>T	NP_001334637.1:n.-398A>T
XM_011544389.2:c.-395A>T	XP_011542691.1:n.-395A>T
NM_000742.4:c.64A>T MANE Select	NP_000733.2:p.Thr22Ser
NM_001282455.2:c.64A>T	NP_001269384.1:p.Thr22Ser
NM_001347705.2:c.-364A>T	NP_001334634.1:n.-364A>T
NM_001347706.2:c.-409A>T	NP_001334635.1:n.-409A>T
NM_001347707.2:c.-350A>T	NP_001334636.1:n.-350A>T
NM_001347708.2:c.-398A>T	NP_001334637.1:n.-398A>T