Canonical Allele Identifier: CA1141581095

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879234T= , CM000663.2:g.156879234T=	GRCh38
NC_000001.10:g.156849026T= , CM000663.1:g.156849026T=	GRCh37
NC_000001.9:g.155115650T=	NCBI36
NG_007493.1:g.68485T= , LRG_261:g.68485T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1738T=	ENSP00000502725.1:p.Tyr580=
ENST00000392302.7:c.1738T=	ENSP00000376120.3:p.Tyr580=
ENST00000497019.7:c.*510T=	ENSP00000436804.2:n.*510T=
ENST00000524377.7:c.1918T= MANE Select	ENSP00000431418.1:p.Tyr640=
ENST00000674537.1:c.1738T=	ENSP00000502725.1:p.Tyr580=
ENST00000358660.3:c.1909T=	ENSP00000351486.3:p.Tyr637=
ENST00000368196.7:c.1900T=	ENSP00000357179.3:p.Tyr634=
ENST00000392302.6:c.1810T=	ENSP00000376120.2:p.Tyr604=
ENST00000497019.6:c.*510T=	ENSP00000436804.1:n.*510T=
ENST00000524377.5:c.1918T=	ENSP00000431418.1:p.Tyr640=
ENST00000530298.5:n.2371T=
NM_001007792.1:c.1810T= , LRG_261t1:c.1810T=	NP_001007793.1:p.Tyr604=
NM_001012331.1:c.1900T= , LRG_261t2:c.1900T=	NP_001012331.1:p.Tyr634=
NM_002529.3:c.1918T= , LRG_261t3:c.1918T=	NP_002520.2:p.Tyr640=
NM_001012331.2:c.1900T=	NP_001012331.1:p.Tyr634=
NM_002529.4:c.1918T= MANE Select	NP_002520.2:p.Tyr640=