Canonical Allele Identifier: CA1974638

Gene: CHRNA1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174757998C>T , CM000664.2:g.174757998C>T	GRCh38
NC_000002.11:g.175622726C>T , CM000664.1:g.175622726C>T	GRCh37
NC_000002.10:g.175330972C>T	NCBI36
NG_008172.1:g.11475G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.-255-323G>A	ENSP00000490338.2:n.-255-323G>A
ENST00000672640.1:c.-255-323G>A	ENSP00000500507.1:n.-255-323G>A
ENST00000261007.9:c.257G>A	ENSP00000261007.5:p.Arg86His
ENST00000348749.9:c.235-323G>A MANE Select	ENSP00000261008.5:n.235-323G>A
ENST00000409219.5:c.235-323G>A	ENSP00000386611.1:n.235-323G>A
ENST00000409323.1:c.235-323G>A	ENSP00000386684.1:n.235-323G>A
ENST00000409542.5:c.234+1333G>A	ENSP00000387026.1:n.234+1333G>A
ENST00000435083.5:c.234+1333G>A	ENSP00000395805.1:n.234+1333G>A
NM_000079.3:c.235-323G>A	NP_000070.1:n.235-323G>A
NM_001039523.2:c.257G>A	NP_001034612.1:p.Arg86His
XM_017003256.1:c.278G>A	XP_016858745.1:p.Arg93His
XM_017003257.1:c.256-323G>A	XP_016858746.1:n.256-323G>A
NM_000079.4:c.235-323G>A MANE Select	NP_000070.1:n.235-323G>A
NM_001039523.3:c.257G>A	NP_001034612.1:p.Arg86His