Canonical Allele Identifier: CA1200784165

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879837C= , CM000663.2:g.156879837C=	GRCh38
NC_000001.10:g.156849629C= , CM000663.1:g.156849629C=	GRCh37
NC_000001.9:g.155116253C=	NCBI36
NG_007493.1:g.69088C= , LRG_261:g.69088C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1867-162C=	ENSP00000502725.1:n.1867-162C=
ENST00000392302.7:c.1867-162C=	ENSP00000376120.3:n.1867-162C=
ENST00000497019.7:c.*639-162C=	ENSP00000436804.2:n.*639-162C=
ENST00000524377.7:c.2047-162C= MANE Select	ENSP00000431418.1:n.2047-162C=
ENST00000531606.2:c.15-162C=
ENST00000674537.1:c.1867-162C=	ENSP00000502725.1:n.1867-162C=
ENST00000358660.3:c.2038-162C=	ENSP00000351486.3:n.2038-162C=
ENST00000368196.7:c.2029-162C=	ENSP00000357179.3:n.2029-162C=
ENST00000392302.6:c.1939-162C=	ENSP00000376120.2:n.1939-162C=
ENST00000497019.6:c.*639-162C=	ENSP00000436804.1:n.*639-162C=
ENST00000524377.5:c.2047-162C=	ENSP00000431418.1:n.2047-162C=
ENST00000530298.5:n.2500-162C=
NM_001007792.1:c.1939-162C= , LRG_261t1:c.1939-162C=	NP_001007793.1:n.1939-162C=
NM_001012331.1:c.2029-162C= , LRG_261t2:c.2029-162C=	NP_001012331.1:n.2029-162C=
NM_002529.3:c.2047-162C= , LRG_261t3:c.2047-162C=	NP_002520.2:n.2047-162C=
NM_001012331.2:c.2029-162C=	NP_001012331.1:n.2029-162C=
NM_002529.4:c.2047-162C= MANE Select	NP_002520.2:n.2047-162C=