Canonical Allele Identifier: CA349335984

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175614688T>A (hg19) ; chr2:g.174749960T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174749960T>A , CM000664.2:g.174749960T>A	GRCh38
NC_000002.11:g.175614688T>A , CM000664.1:g.175614688T>A	GRCh37
NC_000002.10:g.175322934T>A	NCBI36
NG_008172.1:g.19513A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.499A>T	ENSP00000490338.2:p.Asn167Tyr
ENST00000672640.1:c.499A>T	ENSP00000500507.1:p.Asn167Tyr
ENST00000261007.9:c.1063A>T	ENSP00000261007.5:p.Asn355Tyr
ENST00000348749.9:c.988A>T MANE Select	ENSP00000261008.5:p.Asn330Tyr
ENST00000409219.5:c.988A>T	ENSP00000386611.1:p.Asn330Tyr
ENST00000409542.5:c.742A>T	ENSP00000387026.1:p.Asn248Tyr
ENST00000435083.5:c.*632A>T	ENSP00000395805.1:n.*632A>T
NM_000079.3:c.988A>T	NP_000070.1:p.Asn330Tyr
NM_001039523.2:c.1063A>T	NP_001034612.1:p.Asn355Tyr
XM_017003256.1:c.1084A>T	XP_016858745.1:p.Asn362Tyr
XM_017003257.1:c.1009A>T	XP_016858746.1:p.Asn337Tyr
NM_000079.4:c.988A>T MANE Select	NP_000070.1:p.Asn330Tyr
NM_001039523.3:c.1063A>T	NP_001034612.1:p.Asn355Tyr