Canonical Allele Identifier: CA342939757

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1738T>A	ENSP00000502725.1:p.Tyr580Asn
ENST00000392302.7:c.1738T>A	ENSP00000376120.3:p.Tyr580Asn
ENST00000497019.7:c.*510T>A	ENSP00000436804.2:n.*510T>A
ENST00000524377.7:c.1918T>A MANE Select	ENSP00000431418.1:p.Tyr640Asn
ENST00000674537.1:c.1738T>A	ENSP00000502725.1:p.Tyr580Asn
ENST00000358660.3:c.1909T>A	ENSP00000351486.3:p.Tyr637Asn
ENST00000368196.7:c.1900T>A	ENSP00000357179.3:p.Tyr634Asn
ENST00000392302.6:c.1810T>A	ENSP00000376120.2:p.Tyr604Asn
ENST00000497019.6:c.*510T>A	ENSP00000436804.1:n.*510T>A
ENST00000524377.5:c.1918T>A	ENSP00000431418.1:p.Tyr640Asn
ENST00000530298.5:n.2371T>A
NM_001007792.1:c.1810T>A , LRG_261t1:c.1810T>A	NP_001007793.1:p.Tyr604Asn
NM_001012331.1:c.1900T>A , LRG_261t2:c.1900T>A	NP_001012331.1:p.Tyr634Asn
NM_002529.3:c.1918T>A , LRG_261t3:c.1918T>A	NP_002520.2:p.Tyr640Asn
NM_001012331.2:c.1900T>A	NP_001012331.1:p.Tyr634Asn
NM_002529.4:c.1918T>A MANE Select	NP_002520.2:p.Tyr640Asn