Canonical Allele Identifier: CA370810777

Gene: CHRNA2

Linked Data

• MyVariant Identifiers: chr8:g.27321191A>C (hg19) ; chr8:g.27463674A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463674A>C , CM000670.2:g.27463674A>C	GRCh38
NC_000008.10:g.27321191A>C , CM000670.1:g.27321191A>C	GRCh37
NC_000008.9:g.27377108A>C	NCBI36
NG_015827.1:g.20623T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000407991.3:c.769T>G MANE Select	ENSP00000385026.1:p.Tyr257Asp
ENST00000637241.1:c.*599T>G	ENSP00000490690.1:n.*599T>G
ENST00000240132.7:c.724T>G	ENSP00000240132.2:p.Tyr242Asp
ENST00000407991.2:c.769T>G	ENSP00000385026.1:p.Tyr257Asp
ENST00000520600.1:n.290-1920T>G
ENST00000520933.7:c.703T>G	ENSP00000429616.2:p.Tyr235Asp
ENST00000522008.1:n.499T>G
ENST00000523695.5:c.*171T>G	ENSP00000430612.1:n.*171T>G
NM_000742.3:c.769T>G	NP_000733.2:p.Tyr257Asp
NM_001282455.1:c.724T>G	NP_001269384.1:p.Tyr242Asp
XM_005273397.1:c.292T>G	XP_005273454.1:p.Tyr98Asp
XM_006716282.1:c.769T>G	XP_006716345.1:p.Tyr257Asp
XM_011544388.1:c.769T>G	XP_011542690.1:p.Tyr257Asp
XM_011544389.1:c.175T>G	XP_011542691.1:p.Tyr59Asp
NM_001347705.1:c.292T>G	NP_001334634.1:p.Tyr98Asp
NM_001347706.1:c.292T>G	NP_001334635.1:p.Tyr98Asp
NM_001347707.1:c.175T>G	NP_001334636.1:p.Tyr59Asp
NM_001347708.1:c.175T>G	NP_001334637.1:p.Tyr59Asp
XM_011544389.2:c.175T>G	XP_011542691.1:p.Tyr59Asp
NM_000742.4:c.769T>G MANE Select	NP_000733.2:p.Tyr257Asp
NM_001282455.2:c.724T>G	NP_001269384.1:p.Tyr242Asp
NM_001347705.2:c.292T>G	NP_001334634.1:p.Tyr98Asp
NM_001347706.2:c.292T>G	NP_001334635.1:p.Tyr98Asp
NM_001347707.2:c.175T>G	NP_001334636.1:p.Tyr59Asp
NM_001347708.2:c.175T>G	NP_001334637.1:p.Tyr59Asp