Canonical Allele Identifier: CA397297289

Gene: CHRNE

Linked Data

• MyVariant Identifiers: chr17:g.4802062T>A (hg19) ; chr17:g.4898767T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898767T>A , CM000679.2:g.4898767T>A	GRCh38
NC_000017.10:g.4802062T>A , CM000679.1:g.4802062T>A	GRCh37
NC_000017.9:g.4742841T>A	NCBI36
NG_008029.2:g.9309A>T
NG_028005.1:g.70428T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1451A>T MANE Select	ENSP00000497829.1:p.Asp484Val
ENST00000649830.1:c.*87A>T	ENSP00000496907.1:n.*87A>T
ENST00000652550.1:n.1177A>T
ENST00000293780.4:c.1451A>T	ENSP00000293780.4:p.Asp484Val
ENST00000572438.1:n.1137A>T
NM_000080.3:c.1451A>T	NP_000071.1:p.Asp484Val
NM_000080.4:c.1451A>T MANE Select	NP_000071.1:p.Asp484Val
XM_017024115.1:c.1415A>T	XP_016879604.1:p.Asp472Val