Canonical Allele Identifier: CA370808983

Gene: CHRNA2

Linked Data

• gnomAD v4: 8-27463163-C-G
• MyVariant Identifiers: chr8:g.27320680C>G (hg19) ; chr8:g.27463163C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463163C>G , CM000670.2:g.27463163C>G	GRCh38
NC_000008.10:g.27320680C>G , CM000670.1:g.27320680C>G	GRCh37
NC_000008.9:g.27376597C>G	NCBI36
NG_015827.1:g.21134G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1280G>C MANE Select	ENSP00000385026.1:p.Gly427Ala
ENST00000240132.7:c.1235G>C	ENSP00000240132.2:p.Gly412Ala
ENST00000407991.2:c.1280G>C	ENSP00000385026.1:p.Gly427Ala
ENST00000520600.1:n.290-1409G>C
ENST00000520933.7:c.1214G>C	ENSP00000429616.2:p.Gly405Ala
ENST00000523695.5:c.*682G>C	ENSP00000430612.1:n.*682G>C
NM_000742.3:c.1280G>C	NP_000733.2:p.Gly427Ala
NM_001282455.1:c.1235G>C	NP_001269384.1:p.Gly412Ala
XM_005273397.1:c.803G>C	XP_005273454.1:p.Gly268Ala
XM_006716282.1:c.1280G>C	XP_006716345.1:p.Gly427Ala
XM_011544388.1:c.1280G>C	XP_011542690.1:p.Gly427Ala
XM_011544389.1:c.686G>C	XP_011542691.1:p.Gly229Ala
NM_001347705.1:c.803G>C	NP_001334634.1:p.Gly268Ala
NM_001347706.1:c.803G>C	NP_001334635.1:p.Gly268Ala
NM_001347707.1:c.686G>C	NP_001334636.1:p.Gly229Ala
NM_001347708.1:c.686G>C	NP_001334637.1:p.Gly229Ala
XM_011544389.2:c.686G>C	XP_011542691.1:p.Gly229Ala
NM_000742.4:c.1280G>C MANE Select	NP_000733.2:p.Gly427Ala
NM_001282455.2:c.1235G>C	NP_001269384.1:p.Gly412Ala
NM_001347705.2:c.803G>C	NP_001334634.1:p.Gly268Ala
NM_001347706.2:c.803G>C	NP_001334635.1:p.Gly268Ala
NM_001347707.2:c.686G>C	NP_001334636.1:p.Gly229Ala
NM_001347708.2:c.686G>C	NP_001334637.1:p.Gly229Ala