Canonical Allele Identifier: CA349336321

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175614756G>T (hg19) ; chr2:g.174750028G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750028G>T , CM000664.2:g.174750028G>T	GRCh38
NC_000002.11:g.175614756G>T , CM000664.1:g.175614756G>T	GRCh37
NC_000002.10:g.175323002G>T	NCBI36
NG_008172.1:g.19445C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636168.2:c.431C>A	ENSP00000490338.2:p.Ala144Asp
ENST00000672640.1:c.431C>A	ENSP00000500507.1:p.Ala144Asp
ENST00000261007.9:c.995C>A	ENSP00000261007.5:p.Ala332Asp
ENST00000348749.9:c.920C>A MANE Select	ENSP00000261008.5:p.Ala307Asp
ENST00000409219.5:c.920C>A	ENSP00000386611.1:p.Ala307Asp
ENST00000409542.5:c.674C>A	ENSP00000387026.1:p.Ala225Asp
ENST00000435083.5:c.*564C>A	ENSP00000395805.1:n.*564C>A
NM_000079.3:c.920C>A	NP_000070.1:p.Ala307Asp
NM_001039523.2:c.995C>A	NP_001034612.1:p.Ala332Asp
XM_017003256.1:c.1016C>A	XP_016858745.1:p.Ala339Asp
XM_017003257.1:c.941C>A	XP_016858746.1:p.Ala314Asp
NM_000079.4:c.920C>A MANE Select	NP_000070.1:p.Ala307Asp
NM_001039523.3:c.995C>A	NP_001034612.1:p.Ala332Asp