Canonical Allele Identifier: CA393575620

Gene: CHRNA5

Linked Data

• gnomAD v4: 15-78586644-G-T
• MyVariant Identifiers: chr15:g.78878986G>T (hg19) ; chr15:g.78586644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78586644G>T , CM000677.2:g.78586644G>T	GRCh38
NC_000015.9:g.78878986G>T , CM000677.1:g.78878986G>T	GRCh37
NC_000015.8:g.76666041G>T	NCBI36
NG_023328.1:g.26125G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.259-1G>T MANE Select	ENSP00000299565.5:n.259-1G>T
ENST00000394802.4:c.74-1G>T
ENST00000559554.5:c.259-1G>T	ENSP00000453519.1:n.259-1G>T
NM_000745.3:c.259-1G>T	NP_000736.2:n.259-1G>T
NM_001307945.1:c.259-1G>T	NP_001294874.1:n.259-1G>T
XM_005254142.2:c.259-1G>T	XP_005254199.1:n.259-1G>T
NM_001307945.2:c.259-1G>T	NP_001294874.1:n.259-1G>T
NM_000745.4:c.259-1G>T MANE Select	NP_000736.2:n.259-1G>T
NM_001395171.1:c.259-1G>T	NP_001382100.1:n.259-1G>T
NM_001395172.1:c.259-1G>T	NP_001382101.1:n.259-1G>T
NM_001395173.1:c.259-1G>T	NP_001382102.1:n.259-1G>T
NM_001395174.1:c.259-1G>T	NP_001382103.1:n.259-1G>T
NM_001395175.1:c.256-1G>T	NP_001382104.1:n.256-1G>T