Canonical Allele Identifier: CA1141581096

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880036C= , CM000663.2:g.156880036C=	GRCh38
NC_000001.10:g.156849828C= , CM000663.1:g.156849828C=	GRCh37
NC_000001.9:g.155116452C=	NCBI36
NG_007493.1:g.69287C= , LRG_261:g.69287C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1904C=	ENSP00000502725.1:p.Pro635=
ENST00000392302.7:c.1904C=	ENSP00000376120.3:p.Pro635=
ENST00000497019.7:c.*676C=	ENSP00000436804.2:n.*676C=
ENST00000524377.7:c.2084C= MANE Select	ENSP00000431418.1:p.Pro695=
ENST00000531606.2:c.52C=
ENST00000674537.1:c.1904C=	ENSP00000502725.1:p.Pro635=
ENST00000358660.3:c.2075C=	ENSP00000351486.3:p.Pro692=
ENST00000368196.7:c.2066C=	ENSP00000357179.3:p.Pro689=
ENST00000392302.6:c.1976C=	ENSP00000376120.2:p.Pro659=
ENST00000497019.6:c.*676C=	ENSP00000436804.1:n.*676C=
ENST00000524377.5:c.2084C=	ENSP00000431418.1:p.Pro695=
ENST00000530298.5:n.2537C=
ENST00000531606.1:n.36C=
NM_001007792.1:c.1976C= , LRG_261t1:c.1976C=	NP_001007793.1:p.Pro659=
NM_001012331.1:c.2066C= , LRG_261t2:c.2066C=	NP_001012331.1:p.Pro689=
NM_002529.3:c.2084C= , LRG_261t3:c.2084C=	NP_002520.2:p.Pro695=
NM_001012331.2:c.2066C=	NP_001012331.1:p.Pro689=
NM_002529.4:c.2084C= MANE Select	NP_002520.2:p.Pro695=