Canonical Allele Identifier: CA1139846338

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860987G= , CM000663.2:g.156860987G=	GRCh38
NC_000001.10:g.156830779G= , CM000663.1:g.156830779G=	GRCh37
NC_000001.9:g.155097403G=	NCBI36
NG_007493.1:g.50238G= , LRG_261:g.50238G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3367G=	ENSP00000502725.1:n.51-3367G=
ENST00000392302.7:c.51-3367G=	ENSP00000376120.3:n.51-3367G=
ENST00000497019.7:c.51-3367G=	ENSP00000436804.2:n.51-3367G=
ENST00000524377.7:c.53G= MANE Select	ENSP00000431418.1:p.Gly18=
ENST00000674537.1:c.51-3367G=	ENSP00000502725.1:n.51-3367G=
ENST00000675461.1:c.53G=	ENSP00000501668.1:p.Gly18=
ENST00000358660.3:c.53G=	ENSP00000351486.3:p.Gly18=
ENST00000368196.7:c.53G=	ENSP00000357179.3:p.Gly18=
ENST00000392302.6:c.123-3367G=	ENSP00000376120.2:n.123-3367G=
ENST00000489021.6:n.313-12646G=
ENST00000497019.6:c.123-3367G=	ENSP00000436804.1:n.123-3367G=
ENST00000524377.5:c.53G=	ENSP00000431418.1:p.Gly18=
ENST00000530298.5:n.271-3367G=
ENST00000533630.1:n.75G=
NM_001007792.1:c.123-3367G= , LRG_261t1:c.123-3367G=	NP_001007793.1:n.123-3367G=
NM_001012331.1:c.53G= , LRG_261t2:c.53G=	NP_001012331.1:p.Gly18=
NM_002529.3:c.53G= , LRG_261t3:c.53G=	NP_002520.2:p.Gly18=
NM_001012331.2:c.53G=	NP_001012331.1:p.Gly18=
NM_002529.4:c.53G= MANE Select	NP_002520.2:p.Gly18=