Canonical Allele Identifier: CA2740090266

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 3021842
• ClinVar RCV Id: RCV003880425

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156868136dup , CM000663.2:g.156868136dup	GRCh38
NC_000001.10:g.156837928dup , CM000663.1:g.156837928dup	GRCh37
NC_000001.9:g.155104552dup	NCBI36
NG_007493.1:g.57387dup , LRG_261:g.57387dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.299dup	ENSP00000502725.1:p.Cys100TrpfsTer19
ENST00000392302.7:c.299dup	ENSP00000376120.3:p.Cys100TrpfsTer19
ENST00000497019.7:c.299dup	ENSP00000436804.2:p.Cys100TrpfsTer19
ENST00000524377.7:c.461dup MANE Select	ENSP00000431418.1:p.Cys154TrpfsTer19
ENST00000674537.1:c.299dup	ENSP00000502725.1:p.Cys100TrpfsTer19
ENST00000358660.3:c.461dup	ENSP00000351486.3:p.Cys154TrpfsTer19
ENST00000368196.7:c.461dup	ENSP00000357179.3:p.Cys154TrpfsTer19
ENST00000392302.6:c.371dup	ENSP00000376120.2:p.Cys124TrpfsTer19
ENST00000489021.6:n.313-5497dup
ENST00000497019.6:c.371dup	ENSP00000436804.1:p.Cys124TrpfsTer19
ENST00000524377.5:c.461dup	ENSP00000431418.1:p.Cys154TrpfsTer19
ENST00000530298.5:n.519dup
NM_001007792.1:c.371dup , LRG_261t1:c.371dup	NP_001007793.1:p.Cys124TrpfsTer19
NM_001012331.1:c.461dup , LRG_261t2:c.461dup	NP_001012331.1:p.Cys154TrpfsTer19
NM_002529.3:c.461dup , LRG_261t3:c.461dup	NP_002520.2:p.Cys154TrpfsTer19
NM_001012331.2:c.461dup	NP_001012331.1:p.Cys154TrpfsTer19
NM_002529.4:c.461dup MANE Select	NP_002520.2:p.Cys154TrpfsTer19