Canonical Allele Identifier: CA1200787242

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879185T= , CM000663.2:g.156879185T=	GRCh38
NC_000001.10:g.156848977T= , CM000663.1:g.156848977T=	GRCh37
NC_000001.9:g.155115601T=	NCBI36
NG_007493.1:g.68436T= , LRG_261:g.68436T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1689T=	ENSP00000502725.1:p.Gly563=
ENST00000392302.7:c.1689T=	ENSP00000376120.3:p.Gly563=
ENST00000497019.7:c.*461T=	ENSP00000436804.2:n.*461T=
ENST00000524377.7:c.1869T= MANE Select	ENSP00000431418.1:p.Gly623=
ENST00000674537.1:c.1689T=	ENSP00000502725.1:p.Gly563=
ENST00000358660.3:c.1860T=	ENSP00000351486.3:p.Gly620=
ENST00000368196.7:c.1851T=	ENSP00000357179.3:p.Gly617=
ENST00000392302.6:c.1761T=	ENSP00000376120.2:p.Gly587=
ENST00000497019.6:c.*461T=	ENSP00000436804.1:n.*461T=
ENST00000524377.5:c.1869T=	ENSP00000431418.1:p.Gly623=
ENST00000530298.5:n.2322T=
NM_001007792.1:c.1761T= , LRG_261t1:c.1761T=	NP_001007793.1:p.Gly587=
NM_001012331.1:c.1851T= , LRG_261t2:c.1851T=	NP_001012331.1:p.Gly617=
NM_002529.3:c.1869T= , LRG_261t3:c.1869T=	NP_002520.2:p.Gly623=
NM_001012331.2:c.1851T=	NP_001012331.1:p.Gly617=
NM_002529.4:c.1869T= MANE Select	NP_002520.2:p.Gly623=