Canonical Allele Identifier: CA1200787231

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879156G= , CM000663.2:g.156879156G=	GRCh38
NC_000001.10:g.156848948G= , CM000663.1:g.156848948G=	GRCh37
NC_000001.9:g.155115572G=	NCBI36
NG_007493.1:g.68407G= , LRG_261:g.68407G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1660G=	ENSP00000502725.1:p.Gly554=
ENST00000392302.7:c.1660G=	ENSP00000376120.3:p.Gly554=
ENST00000497019.7:c.*432G=	ENSP00000436804.2:n.*432G=
ENST00000524377.7:c.1840G= MANE Select	ENSP00000431418.1:p.Gly614=
ENST00000674537.1:c.1660G=	ENSP00000502725.1:p.Gly554=
ENST00000358660.3:c.1831G=	ENSP00000351486.3:p.Gly611=
ENST00000368196.7:c.1822G=	ENSP00000357179.3:p.Gly608=
ENST00000392302.6:c.1732G=	ENSP00000376120.2:p.Gly578=
ENST00000497019.6:c.*432G=	ENSP00000436804.1:n.*432G=
ENST00000524377.5:c.1840G=	ENSP00000431418.1:p.Gly614=
ENST00000530298.5:n.2293G=
NM_001007792.1:c.1732G= , LRG_261t1:c.1732G=	NP_001007793.1:p.Gly578=
NM_001012331.1:c.1822G= , LRG_261t2:c.1822G=	NP_001012331.1:p.Gly608=
NM_002529.3:c.1840G= , LRG_261t3:c.1840G=	NP_002520.2:p.Gly614=
NM_001012331.2:c.1822G=	NP_001012331.1:p.Gly608=
NM_002529.4:c.1840G= MANE Select	NP_002520.2:p.Gly614=