Canonical Allele Identifier: CA397297194

Gene: CHRNE

Linked Data

• gnomAD v4: 17-4898749-C-T
• MyVariant Identifiers: chr17:g.4802044C>T (hg19) ; chr17:g.4898749C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898749C>T , CM000679.2:g.4898749C>T	GRCh38
NC_000017.10:g.4802044C>T , CM000679.1:g.4802044C>T	GRCh37
NC_000017.9:g.4742823C>T	NCBI36
NG_008029.2:g.9327G>A
NG_028005.1:g.70410C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1469G>A MANE Select	ENSP00000497829.1:p.Cys490Tyr
ENST00000649830.1:c.*105G>A	ENSP00000496907.1:n.*105G>A
ENST00000652550.1:n.1195G>A
ENST00000293780.4:c.1469G>A	ENSP00000293780.4:p.Cys490Tyr
ENST00000572438.1:n.1155G>A
NM_000080.3:c.1469G>A	NP_000071.1:p.Cys490Tyr
NM_000080.4:c.1469G>A MANE Select	NP_000071.1:p.Cys490Tyr
XM_017024115.1:c.1433G>A	XP_016879604.1:p.Cys478Tyr