Canonical Allele Identifier: CA31113433

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156871747A>G , CM000663.2:g.156871747A>G	GRCh38
NC_000001.10:g.156841539A>G , CM000663.1:g.156841539A>G	GRCh37
NC_000001.9:g.155108163A>G	NCBI36
NG_007493.1:g.60998A>G , LRG_261:g.60998A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.680A>G	ENSP00000502725.1:p.Asn227Ser
ENST00000392302.7:c.680A>G	ENSP00000376120.3:p.Asn227Ser
ENST00000497019.7:c.556-1886A>G	ENSP00000436804.2:n.556-1886A>G
ENST00000524377.7:c.842A>G MANE Select	ENSP00000431418.1:p.Asn281Ser
ENST00000674537.1:c.680A>G	ENSP00000502725.1:p.Asn227Ser
ENST00000358660.3:c.842A>G	ENSP00000351486.3:p.Asn281Ser
ENST00000368196.7:c.842A>G	ENSP00000357179.3:p.Asn281Ser
ENST00000392302.6:c.752A>G	ENSP00000376120.2:p.Asn251Ser
ENST00000489021.6:n.313-1886A>G
ENST00000497019.6:c.628-1886A>G	ENSP00000436804.1:n.628-1886A>G
ENST00000524377.5:c.842A>G	ENSP00000431418.1:p.Asn281Ser
ENST00000530298.5:n.900A>G
NM_001007792.1:c.752A>G , LRG_261t1:c.752A>G	NP_001007793.1:p.Asn251Ser
NM_001012331.1:c.842A>G , LRG_261t2:c.842A>G	NP_001012331.1:p.Asn281Ser
NM_002529.3:c.842A>G , LRG_261t3:c.842A>G	NP_002520.2:p.Asn281Ser
NM_001012331.2:c.842A>G	NP_001012331.1:p.Asn281Ser
NM_002529.4:c.842A>G MANE Select	NP_002520.2:p.Asn281Ser