Canonical Allele Identifier: CA1200785948

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876193A= , CM000663.2:g.156876193A=	GRCh38
NC_000001.10:g.156845985A= , CM000663.1:g.156845985A=	GRCh37
NC_000001.9:g.155112609A=	NCBI36
NG_007493.1:g.65444A= , LRG_261:g.65444A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1435A=	ENSP00000502725.1:p.Met479=
ENST00000392302.7:c.1435A=	ENSP00000376120.3:p.Met479=
ENST00000497019.7:c.*207A=	ENSP00000436804.2:n.*207A=
ENST00000524377.7:c.1615A= MANE Select	ENSP00000431418.1:p.Met539=
ENST00000674537.1:c.1435A=	ENSP00000502725.1:p.Met479=
ENST00000358660.3:c.1606A=	ENSP00000351486.3:p.Met536=
ENST00000368196.7:c.1597A=	ENSP00000357179.3:p.Met533=
ENST00000392302.6:c.1507A=	ENSP00000376120.2:p.Met503=
ENST00000497019.6:c.*207A=	ENSP00000436804.1:n.*207A=
ENST00000524377.5:c.1615A=	ENSP00000431418.1:p.Met539=
ENST00000530298.5:n.2068A=
ENST00000534682.1:n.838A=
NM_001007792.1:c.1507A= , LRG_261t1:c.1507A=	NP_001007793.1:p.Met503=
NM_001012331.1:c.1597A= , LRG_261t2:c.1597A=	NP_001012331.1:p.Met533=
NM_002529.3:c.1615A= , LRG_261t3:c.1615A=	NP_002520.2:p.Met539=
NM_001012331.2:c.1597A=	NP_001012331.1:p.Met533=
NM_002529.4:c.1615A= MANE Select	NP_002520.2:p.Met539=