Canonical Allele Identifier: CA1169582

Gene: NTRK1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880121C>T , CM000663.2:g.156880121C>T	GRCh38
NC_000001.10:g.156849913C>T , CM000663.1:g.156849913C>T	GRCh37
NC_000001.9:g.155116537C>T	NCBI36
NG_007493.1:g.69372C>T , LRG_261:g.69372C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1989C>T	ENSP00000502725.1:p.Tyr663=
ENST00000392302.7:c.1989C>T	ENSP00000376120.3:p.Tyr663=
ENST00000497019.7:c.*761C>T	ENSP00000436804.2:n.*761C>T
ENST00000524377.7:c.2169C>T MANE Select	ENSP00000431418.1:p.Tyr723=
ENST00000531606.2:c.137C>T
ENST00000674537.1:c.1989C>T	ENSP00000502725.1:p.Tyr663=
ENST00000358660.3:c.2160C>T	ENSP00000351486.3:p.Tyr720=
ENST00000368196.7:c.2151C>T	ENSP00000357179.3:p.Tyr717=
ENST00000392302.6:c.2061C>T	ENSP00000376120.2:p.Tyr687=
ENST00000497019.6:c.*761C>T	ENSP00000436804.1:n.*761C>T
ENST00000524377.5:c.2169C>T	ENSP00000431418.1:p.Tyr723=
ENST00000530298.5:n.2622C>T
ENST00000531606.1:n.121C>T
NM_001007792.1:c.2061C>T , LRG_261t1:c.2061C>T	NP_001007793.1:p.Tyr687=
NM_001012331.1:c.2151C>T , LRG_261t2:c.2151C>T	NP_001012331.1:p.Tyr717=
NM_002529.3:c.2169C>T , LRG_261t3:c.2169C>T	NP_002520.2:p.Tyr723=
NM_001012331.2:c.2151C>T	NP_001012331.1:p.Tyr717=
NM_002529.4:c.2169C>T MANE Select	NP_002520.2:p.Tyr723=