Canonical Allele Identifier: CA1200789016

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881615T= , CM000663.2:g.156881615T=	GRCh38
NC_000001.10:g.156851407T= , CM000663.1:g.156851407T=	GRCh37
NC_000001.9:g.155118031T=	NCBI36
NG_007493.1:g.70866T= , LRG_261:g.70866T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2184T=	ENSP00000502725.1:p.Pro728=
ENST00000392302.7:c.2184T=	ENSP00000376120.3:p.Pro728=
ENST00000497019.7:c.*956T=	ENSP00000436804.2:n.*956T=
ENST00000524377.7:c.2364T= MANE Select	ENSP00000431418.1:p.Pro788=
ENST00000531606.2:c.423T=
ENST00000674537.1:c.2184T=	ENSP00000502725.1:p.Pro728=
ENST00000358660.3:c.2355T=	ENSP00000351486.3:p.Pro785=
ENST00000368196.7:c.2346T=	ENSP00000357179.3:p.Pro782=
ENST00000392302.6:c.2256T=	ENSP00000376120.2:p.Pro752=
ENST00000497019.6:c.*956T=	ENSP00000436804.1:n.*956T=
ENST00000524377.5:c.2364T=	ENSP00000431418.1:p.Pro788=
ENST00000530298.5:n.2817T=
ENST00000531606.1:n.407T=
NM_001007792.1:c.2256T= , LRG_261t1:c.2256T=	NP_001007793.1:p.Pro752=
NM_001012331.1:c.2346T= , LRG_261t2:c.2346T=	NP_001012331.1:p.Pro782=
NM_002529.3:c.2364T= , LRG_261t3:c.2364T=	NP_002520.2:p.Pro788=
NM_001012331.2:c.2346T=	NP_001012331.1:p.Pro782=
NM_002529.4:c.2364T= MANE Select	NP_002520.2:p.Pro788=