Canonical Allele Identifier: CA1200785934

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876150C= , CM000663.2:g.156876150C=	GRCh38
NC_000001.10:g.156845942C= , CM000663.1:g.156845942C=	GRCh37
NC_000001.9:g.155112566C=	NCBI36
NG_007493.1:g.65401C= , LRG_261:g.65401C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1392C=	ENSP00000502725.1:p.Val464=
ENST00000392302.7:c.1392C=	ENSP00000376120.3:p.Val464=
ENST00000497019.7:c.*164C=	ENSP00000436804.2:n.*164C=
ENST00000524377.7:c.1572C= MANE Select	ENSP00000431418.1:p.Val524=
ENST00000674537.1:c.1392C=	ENSP00000502725.1:p.Val464=
ENST00000358660.3:c.1563C=	ENSP00000351486.3:p.Val521=
ENST00000368196.7:c.1554C=	ENSP00000357179.3:p.Val518=
ENST00000392302.6:c.1464C=	ENSP00000376120.2:p.Val488=
ENST00000497019.6:c.*164C=	ENSP00000436804.1:n.*164C=
ENST00000524377.5:c.1572C=	ENSP00000431418.1:p.Val524=
ENST00000530298.5:n.2025C=
ENST00000534682.1:n.795C=
NM_001007792.1:c.1464C= , LRG_261t1:c.1464C=	NP_001007793.1:p.Val488=
NM_001012331.1:c.1554C= , LRG_261t2:c.1554C=	NP_001012331.1:p.Val518=
NM_002529.3:c.1572C= , LRG_261t3:c.1572C=	NP_002520.2:p.Val524=
NM_001012331.2:c.1554C=	NP_001012331.1:p.Val518=
NM_002529.4:c.1572C= MANE Select	NP_002520.2:p.Val524=