Canonical Allele Identifier: CA1200785670

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875525G= , CM000663.2:g.156875525G=	GRCh38
NC_000001.10:g.156845317G= , CM000663.1:g.156845317G=	GRCh37
NC_000001.9:g.155111941G=	NCBI36
NG_007493.1:g.64776G= , LRG_261:g.64776G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1180G=	ENSP00000502725.1:p.Ala394=
ENST00000392302.7:c.1180G=	ENSP00000376120.3:p.Ala394=
ENST00000497019.7:c.1047G=	ENSP00000436804.2:p.Arg349=
ENST00000524377.7:c.1360G= MANE Select	ENSP00000431418.1:p.Ala454=
ENST00000674537.1:c.1180G=	ENSP00000502725.1:p.Ala394=
ENST00000358660.3:c.1342G=	ENSP00000351486.3:p.Ala448=
ENST00000368196.7:c.1342G=	ENSP00000357179.3:p.Ala448=
ENST00000392302.6:c.1252G=	ENSP00000376120.2:p.Ala418=
ENST00000497019.6:c.1119G=	ENSP00000436804.1:p.Arg373=
ENST00000524377.5:c.1360G=	ENSP00000431418.1:p.Ala454=
ENST00000530298.5:n.1400G=
ENST00000534682.1:n.583G=
NM_001007792.1:c.1252G= , LRG_261t1:c.1252G=	NP_001007793.1:p.Ala418=
NM_001012331.1:c.1342G= , LRG_261t2:c.1342G=	NP_001012331.1:p.Ala448=
NM_002529.3:c.1360G= , LRG_261t3:c.1360G=	NP_002520.2:p.Ala454=
NM_001012331.2:c.1342G=	NP_001012331.1:p.Ala448=
NM_002529.4:c.1360G= MANE Select	NP_002520.2:p.Ala454=