Canonical Allele Identifier: CA2808375228

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454244_7454245insCTGTCTCTT , CM000679.2:g.7454244_7454245insCTGTCTCTT	GRCh38
NC_000017.10:g.7357563_7357564insCTGTCTCTT , CM000679.1:g.7357563_7357564insCTGTCTCTT	GRCh37
NC_000017.9:g.7298287_7298288insCTGTCTCTT	NCBI36
NG_008026.1:g.14158_14159insCTGTCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.821-53_821-52insCTGTCTCTT MANE Select	ENSP00000304290.2:n.821-53_821-52insCTGTCTCTT
ENST00000306071.6:c.821-53_821-52insCTGTCTCTT	ENSP00000304290.2:n.821-53_821-52insCTGTCTCTT
ENST00000536404.6:c.605-53_605-52insCTGTCTCTT	ENSP00000439209.2:n.605-53_605-52insCTGTCTCTT
ENST00000570557.5:c.484-53_484-52insCTGTCTCTT
ENST00000573209.1:n.1765-53_1765-52insCTGTCTCTT
ENST00000576360.1:c.605-200_605-199insCTGTCTCTT	ENSP00000459092.1:n.605-200_605-199insCTGTCTCTT
NM_000747.2:c.821-53_821-52insCTGTCTCTT	NP_000738.2:n.821-53_821-52insCTGTCTCTT
NM_000747.3:c.821-53_821-52insCTGTCTCTT MANE Select	NP_000738.2:n.821-53_821-52insCTGTCTCTT