Canonical Allele Identifier: CA1148263459

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156864742G= , CM000663.2:g.156864742G=	GRCh38
NC_000001.10:g.156834534G= , CM000663.1:g.156834534G=	GRCh37
NC_000001.9:g.155101158G=	NCBI36
NG_007493.1:g.53993G= , LRG_261:g.53993G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.140G=	ENSP00000502725.1:p.Ser47=
ENST00000392302.7:c.140G=	ENSP00000376120.3:p.Ser47=
ENST00000497019.7:c.140G=	ENSP00000436804.2:p.Ser47=
ENST00000524377.7:c.302G= MANE Select	ENSP00000431418.1:p.Ser101=
ENST00000674537.1:c.140G=	ENSP00000502725.1:p.Ser47=
ENST00000675461.1:c.302G=	ENSP00000501668.1:p.Ser101=
ENST00000358660.3:c.302G=	ENSP00000351486.3:p.Ser101=
ENST00000368196.7:c.302G=	ENSP00000357179.3:p.Ser101=
ENST00000392302.6:c.212G=	ENSP00000376120.2:p.Ser71=
ENST00000489021.6:n.313-8891G=
ENST00000497019.6:c.212G=	ENSP00000436804.1:p.Ser71=
ENST00000524377.5:c.302G=	ENSP00000431418.1:p.Ser101=
ENST00000530298.5:n.360G=
ENST00000533630.1:n.324G=
NM_001007792.1:c.212G= , LRG_261t1:c.212G=	NP_001007793.1:p.Ser71=
NM_001012331.1:c.302G= , LRG_261t2:c.302G=	NP_001012331.1:p.Ser101=
NM_002529.3:c.302G= , LRG_261t3:c.302G=	NP_002520.2:p.Ser101=
NM_001012331.2:c.302G=	NP_001012331.1:p.Ser101=
NM_002529.4:c.302G= MANE Select	NP_002520.2:p.Ser101=