Canonical Allele Identifier: CA1200785944

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876180T= , CM000663.2:g.156876180T=	GRCh38
NC_000001.10:g.156845972T= , CM000663.1:g.156845972T=	GRCh37
NC_000001.9:g.155112596T=	NCBI36
NG_007493.1:g.65431T= , LRG_261:g.65431T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1422T=	ENSP00000502725.1:p.Pro474=
ENST00000392302.7:c.1422T=	ENSP00000376120.3:p.Pro474=
ENST00000497019.7:c.*194T=	ENSP00000436804.2:n.*194T=
ENST00000524377.7:c.1602T= MANE Select	ENSP00000431418.1:p.Pro534=
ENST00000674537.1:c.1422T=	ENSP00000502725.1:p.Pro474=
ENST00000358660.3:c.1593T=	ENSP00000351486.3:p.Pro531=
ENST00000368196.7:c.1584T=	ENSP00000357179.3:p.Pro528=
ENST00000392302.6:c.1494T=	ENSP00000376120.2:p.Pro498=
ENST00000497019.6:c.*194T=	ENSP00000436804.1:n.*194T=
ENST00000524377.5:c.1602T=	ENSP00000431418.1:p.Pro534=
ENST00000530298.5:n.2055T=
ENST00000534682.1:n.825T=
NM_001007792.1:c.1494T= , LRG_261t1:c.1494T=	NP_001007793.1:p.Pro498=
NM_001012331.1:c.1584T= , LRG_261t2:c.1584T=	NP_001012331.1:p.Pro528=
NM_002529.3:c.1602T= , LRG_261t3:c.1602T=	NP_002520.2:p.Pro534=
NM_001012331.2:c.1584T=	NP_001012331.1:p.Pro528=
NM_002529.4:c.1602T= MANE Select	NP_002520.2:p.Pro534=