Canonical Allele Identifier: CA10611417

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750180_174750181del , CM000664.2:g.174750180_174750181del	GRCh38
NC_000002.11:g.175614908_175614909del , CM000664.1:g.175614908_175614909del	GRCh37
NC_000002.10:g.175323154_175323155del	NCBI36
NG_008172.1:g.19292_19293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.290-12_290-11del	ENSP00000490338.2:n.290-12_290-11del
ENST00000672640.1:c.290-12_290-11del	ENSP00000500507.1:n.290-12_290-11del
ENST00000261007.9:c.854-12_854-11del	ENSP00000261007.5:n.854-12_854-11del
ENST00000348749.9:c.779-12_779-11del MANE Select	ENSP00000261008.5:n.779-12_779-11del
ENST00000409219.5:c.779-12_779-11del	ENSP00000386611.1:n.779-12_779-11del
ENST00000409542.5:c.533-12_533-11del	ENSP00000387026.1:n.533-12_533-11del
ENST00000435083.5:c.*423-12_*423-11del	ENSP00000395805.1:n.*423-12_*423-11del
NM_000079.3:c.779-12_779-11del	NP_000070.1:n.779-12_779-11del
NM_001039523.2:c.854-12_854-11del	NP_001034612.1:n.854-12_854-11del
XM_017003256.1:c.875-12_875-11del	XP_016858745.1:n.875-12_875-11del
XM_017003257.1:c.800-12_800-11del	XP_016858746.1:n.800-12_800-11del
NM_000079.4:c.779-12_779-11del MANE Select	NP_000070.1:n.779-12_779-11del
NM_001039523.3:c.854-12_854-11del	NP_001034612.1:n.854-12_854-11del