Canonical Allele Identifier: CA342938470

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156846231C>T (hg19) ; chr1:g.156876439C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876439C>T , CM000663.2:g.156876439C>T	GRCh38
NC_000001.10:g.156846231C>T , CM000663.1:g.156846231C>T	GRCh37
NC_000001.9:g.155112855C>T	NCBI36
NG_007493.1:g.65690C>T , LRG_261:g.65690C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1492C>T	ENSP00000502725.1:p.Gln498Ter
ENST00000392302.7:c.1492C>T	ENSP00000376120.3:p.Gln498Ter
ENST00000497019.7:c.*264C>T	ENSP00000436804.2:n.*264C>T
ENST00000524377.7:c.1672C>T MANE Select	ENSP00000431418.1:p.Gln558Ter
ENST00000674537.1:c.1492C>T	ENSP00000502725.1:p.Gln498Ter
ENST00000358660.3:c.1663C>T	ENSP00000351486.3:p.Gln555Ter
ENST00000368196.7:c.1654C>T	ENSP00000357179.3:p.Gln552Ter
ENST00000392302.6:c.1564C>T	ENSP00000376120.2:p.Gln522Ter
ENST00000497019.6:c.*264C>T	ENSP00000436804.1:n.*264C>T
ENST00000524377.5:c.1672C>T	ENSP00000431418.1:p.Gln558Ter
ENST00000530298.5:n.2125C>T
NM_001007792.1:c.1564C>T , LRG_261t1:c.1564C>T	NP_001007793.1:p.Gln522Ter
NM_001012331.1:c.1654C>T , LRG_261t2:c.1654C>T	NP_001012331.1:p.Gln552Ter
NM_002529.3:c.1672C>T , LRG_261t3:c.1672C>T	NP_002520.2:p.Gln558Ter
NM_001012331.2:c.1654C>T	NP_001012331.1:p.Gln552Ter
NM_002529.4:c.1672C>T MANE Select	NP_002520.2:p.Gln558Ter