Canonical Allele Identifier: CA370806981

Gene: CHRNA2

Linked Data

• MyVariant Identifiers: chr8:g.27319210A>T (hg19) ; chr8:g.27461693A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27461693A>T , CM000670.2:g.27461693A>T	GRCh38
NC_000008.10:g.27319210A>T , CM000670.1:g.27319210A>T	GRCh37
NC_000008.9:g.27375127A>T	NCBI36
NG_015827.1:g.22604T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000407991.3:c.1526T>A MANE Select	ENSP00000385026.1:p.Ile509Asn
ENST00000240132.7:c.1481T>A	ENSP00000240132.2:p.Ile494Asn
ENST00000407991.2:c.1526T>A	ENSP00000385026.1:p.Ile509Asn
ENST00000520600.1:n.351T>A
ENST00000520933.7:c.1460T>A	ENSP00000429616.2:p.Ile487Asn
ENST00000523695.5:c.*928T>A	ENSP00000430612.1:n.*928T>A
NM_000742.3:c.1526T>A	NP_000733.2:p.Ile509Asn
NM_001282455.1:c.1481T>A	NP_001269384.1:p.Ile494Asn
XM_005273397.1:c.1049T>A	XP_005273454.1:p.Ile350Asn
XM_006716282.1:c.1526T>A	XP_006716345.1:p.Ile509Asn
XM_011544388.1:c.1526T>A	XP_011542690.1:p.Ile509Asn
XM_011544389.1:c.932T>A	XP_011542691.1:p.Ile311Asn
NM_001347705.1:c.1049T>A	NP_001334634.1:p.Ile350Asn
NM_001347706.1:c.1049T>A	NP_001334635.1:p.Ile350Asn
NM_001347707.1:c.932T>A	NP_001334636.1:p.Ile311Asn
NM_001347708.1:c.932T>A	NP_001334637.1:p.Ile311Asn
XM_011544389.2:c.932T>A	XP_011542691.1:p.Ile311Asn
NM_000742.4:c.1526T>A MANE Select	NP_000733.2:p.Ile509Asn
NM_001282455.2:c.1481T>A	NP_001269384.1:p.Ile494Asn
NM_001347705.2:c.1049T>A	NP_001334634.1:p.Ile350Asn
NM_001347706.2:c.1049T>A	NP_001334635.1:p.Ile350Asn
NM_001347707.2:c.932T>A	NP_001334636.1:p.Ile311Asn
NM_001347708.2:c.932T>A	NP_001334637.1:p.Ile311Asn