Canonical Allele Identifier: CA1140614581

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879130G= , CM000663.2:g.156879130G=	GRCh38
NC_000001.10:g.156848922G= , CM000663.1:g.156848922G=	GRCh37
NC_000001.9:g.155115546G=	NCBI36
NG_007493.1:g.68381G= , LRG_261:g.68381G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1634G=	ENSP00000502725.1:p.Gly545=
ENST00000392302.7:c.1634G=	ENSP00000376120.3:p.Gly545=
ENST00000497019.7:c.*406G=	ENSP00000436804.2:n.*406G=
ENST00000524377.7:c.1814G= MANE Select	ENSP00000431418.1:p.Gly605=
ENST00000674537.1:c.1634G=	ENSP00000502725.1:p.Gly545=
ENST00000358660.3:c.1805G=	ENSP00000351486.3:p.Gly602=
ENST00000368196.7:c.1796G=	ENSP00000357179.3:p.Gly599=
ENST00000392302.6:c.1706G=	ENSP00000376120.2:p.Gly569=
ENST00000497019.6:c.*406G=	ENSP00000436804.1:n.*406G=
ENST00000524377.5:c.1814G=	ENSP00000431418.1:p.Gly605=
ENST00000530298.5:n.2267G=
NM_001007792.1:c.1706G= , LRG_261t1:c.1706G=	NP_001007793.1:p.Gly569=
NM_001012331.1:c.1796G= , LRG_261t2:c.1796G=	NP_001012331.1:p.Gly599=
NM_002529.3:c.1814G= , LRG_261t3:c.1814G=	NP_002520.2:p.Gly605=
NM_001012331.2:c.1796G=	NP_001012331.1:p.Gly599=
NM_002529.4:c.1814G= MANE Select	NP_002520.2:p.Gly605=