Canonical Allele Identifier: CA342940050

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879336G>A , CM000663.2:g.156879336G>A	GRCh38
NC_000001.10:g.156849128G>A , CM000663.1:g.156849128G>A	GRCh37
NC_000001.9:g.155115752G>A	NCBI36
NG_007493.1:g.68587G>A , LRG_261:g.68587G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1840G>A	ENSP00000502725.1:p.Asp614Asn
ENST00000392302.7:c.1840G>A	ENSP00000376120.3:p.Asp614Asn
ENST00000497019.7:c.*612G>A	ENSP00000436804.2:n.*612G>A
ENST00000524377.7:c.2020G>A MANE Select	ENSP00000431418.1:p.Asp674Asn
ENST00000674537.1:c.1840G>A	ENSP00000502725.1:p.Asp614Asn
ENST00000358660.3:c.2011G>A	ENSP00000351486.3:p.Asp671Asn
ENST00000368196.7:c.2002G>A	ENSP00000357179.3:p.Asp668Asn
ENST00000392302.6:c.1912G>A	ENSP00000376120.2:p.Asp638Asn
ENST00000497019.6:c.*612G>A	ENSP00000436804.1:n.*612G>A
ENST00000524377.5:c.2020G>A	ENSP00000431418.1:p.Asp674Asn
ENST00000530298.5:n.2473G>A
NM_001007792.1:c.1912G>A , LRG_261t1:c.1912G>A	NP_001007793.1:p.Asp638Asn
NM_001012331.1:c.2002G>A , LRG_261t2:c.2002G>A	NP_001012331.1:p.Asp668Asn
NM_002529.3:c.2020G>A , LRG_261t3:c.2020G>A	NP_002520.2:p.Asp674Asn
NM_001012331.2:c.2002G>A	NP_001012331.1:p.Asp668Asn
NM_002529.4:c.2020G>A MANE Select	NP_002520.2:p.Asp674Asn