Canonical Allele Identifier: CA342939381

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879126C>G , CM000663.2:g.156879126C>G	GRCh38
NC_000001.10:g.156848918C>G , CM000663.1:g.156848918C>G	GRCh37
NC_000001.9:g.155115542C>G	NCBI36
NG_007493.1:g.68377C>G , LRG_261:g.68377C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1630C>G	ENSP00000502725.1:p.His544Asp
ENST00000392302.7:c.1630C>G	ENSP00000376120.3:p.His544Asp
ENST00000497019.7:c.*402C>G	ENSP00000436804.2:n.*402C>G
ENST00000524377.7:c.1810C>G MANE Select	ENSP00000431418.1:p.His604Asp
ENST00000674537.1:c.1630C>G	ENSP00000502725.1:p.His544Asp
ENST00000358660.3:c.1801C>G	ENSP00000351486.3:p.His601Asp
ENST00000368196.7:c.1792C>G	ENSP00000357179.3:p.His598Asp
ENST00000392302.6:c.1702C>G	ENSP00000376120.2:p.His568Asp
ENST00000497019.6:c.*402C>G	ENSP00000436804.1:n.*402C>G
ENST00000524377.5:c.1810C>G	ENSP00000431418.1:p.His604Asp
ENST00000530298.5:n.2263C>G
NM_001007792.1:c.1702C>G , LRG_261t1:c.1702C>G	NP_001007793.1:p.His568Asp
NM_001012331.1:c.1792C>G , LRG_261t2:c.1792C>G	NP_001012331.1:p.His598Asp
NM_002529.3:c.1810C>G , LRG_261t3:c.1810C>G	NP_002520.2:p.His604Asp
NM_001012331.2:c.1792C>G	NP_001012331.1:p.His598Asp
NM_002529.4:c.1810C>G MANE Select	NP_002520.2:p.His604Asp