Canonical Allele Identifier: CA1200788720

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881508C= , CM000663.2:g.156881508C=	GRCh38
NC_000001.10:g.156851300C= , CM000663.1:g.156851300C=	GRCh37
NC_000001.9:g.155117924C=	NCBI36
NG_007493.1:g.70759C= , LRG_261:g.70759C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2077C=	ENSP00000502725.1:p.Pro693=
ENST00000392302.7:c.2077C=	ENSP00000376120.3:p.Pro693=
ENST00000497019.7:c.*849C=	ENSP00000436804.2:n.*849C=
ENST00000524377.7:c.2257C= MANE Select	ENSP00000431418.1:p.Pro753=
ENST00000531606.2:c.316C=
ENST00000674537.1:c.2077C=	ENSP00000502725.1:p.Pro693=
ENST00000358660.3:c.2248C=	ENSP00000351486.3:p.Pro750=
ENST00000368196.7:c.2239C=	ENSP00000357179.3:p.Pro747=
ENST00000392302.6:c.2149C=	ENSP00000376120.2:p.Pro717=
ENST00000497019.6:c.*849C=	ENSP00000436804.1:n.*849C=
ENST00000524377.5:c.2257C=	ENSP00000431418.1:p.Pro753=
ENST00000530298.5:n.2710C=
ENST00000531606.1:n.300C=
NM_001007792.1:c.2149C= , LRG_261t1:c.2149C=	NP_001007793.1:p.Pro717=
NM_001012331.1:c.2239C= , LRG_261t2:c.2239C=	NP_001012331.1:p.Pro747=
NM_002529.3:c.2257C= , LRG_261t3:c.2257C=	NP_002520.2:p.Pro753=
NM_001012331.2:c.2239C=	NP_001012331.1:p.Pro747=
NM_002529.4:c.2257C= MANE Select	NP_002520.2:p.Pro753=