Canonical Allele Identifier: CA1308832538

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750035C= , CM000664.2:g.174750035C=	GRCh38
NC_000002.11:g.175614763C= , CM000664.1:g.175614763C=	GRCh37
NC_000002.10:g.175323009C=	NCBI36
NG_008172.1:g.19438G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000079.4:c.913G= MANE Select	NP_000070.1:p.Val305=
ENST00000348749.9:c.913G= MANE Select	ENSP00000261008.5:p.Val305=
NM_000079.3:c.913G=	NP_000070.1:p.Val305=
NM_001039523.2:c.988G=	NP_001034612.1:p.Val330=
NM_001039523.3:c.988G=	NP_001034612.1:p.Val330=
ENST00000261007.9:c.988G=	ENSP00000261007.5:p.Val330=
ENST00000409219.5:c.913G=	ENSP00000386611.1:p.Val305=
ENST00000409542.5:c.667G=	ENSP00000387026.1:p.Val223=
ENST00000435083.5:c.*557G=	ENSP00000395805.1:n.*557G=
ENST00000636168.2:c.424G=	ENSP00000490338.2:p.Val142=
ENST00000672640.1:c.424G=	ENSP00000500507.1:p.Val142=
XM_017003256.1:c.1009G=	XP_016858745.1:p.Val337=
XM_017003257.1:c.934G=	XP_016858746.1:p.Val312=