Canonical Allele Identifier: CA1143526763

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875523C= , CM000663.2:g.156875523C=	GRCh38
NC_000001.10:g.156845315C= , CM000663.1:g.156845315C=	GRCh37
NC_000001.9:g.155111939C=	NCBI36
NG_007493.1:g.64774C= , LRG_261:g.64774C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1178C=	ENSP00000502725.1:p.Pro393=
ENST00000392302.7:c.1178C=	ENSP00000376120.3:p.Pro393=
ENST00000497019.7:c.1045C=	ENSP00000436804.2:p.Arg349=
ENST00000524377.7:c.1358C= MANE Select	ENSP00000431418.1:p.Pro453=
ENST00000674537.1:c.1178C=	ENSP00000502725.1:p.Pro393=
ENST00000358660.3:c.1340C=	ENSP00000351486.3:p.Pro447=
ENST00000368196.7:c.1340C=	ENSP00000357179.3:p.Pro447=
ENST00000392302.6:c.1250C=	ENSP00000376120.2:p.Pro417=
ENST00000497019.6:c.1117C=	ENSP00000436804.1:p.Arg373=
ENST00000524377.5:c.1358C=	ENSP00000431418.1:p.Pro453=
ENST00000530298.5:n.1398C=
ENST00000534682.1:n.581C=
NM_001007792.1:c.1250C= , LRG_261t1:c.1250C=	NP_001007793.1:p.Pro417=
NM_001012331.1:c.1340C= , LRG_261t2:c.1340C=	NP_001012331.1:p.Pro447=
NM_002529.3:c.1358C= , LRG_261t3:c.1358C=	NP_002520.2:p.Pro453=
NM_001012331.2:c.1340C=	NP_001012331.1:p.Pro447=
NM_002529.4:c.1358C= MANE Select	NP_002520.2:p.Pro453=