Canonical Allele Identifier: CA421270912

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 2701534
• ClinVar RCV Id: RCV003512820
• COSMIC: COSM81496
• MyVariant Identifiers: chr1:g.156837923T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156868131T>C , CM000663.2:g.156868131T>C	GRCh38
NC_000001.10:g.156837923T>C , CM000663.1:g.156837923T>C	GRCh37
NC_000001.9:g.155104547T>C	NCBI36
NG_007493.1:g.57382T>C , LRG_261:g.57382T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.294T>C	ENSP00000502725.1:p.Cys98=
ENST00000392302.7:c.294T>C	ENSP00000376120.3:p.Cys98=
ENST00000497019.7:c.294T>C	ENSP00000436804.2:p.Cys98=
ENST00000524377.7:c.456T>C MANE Select	ENSP00000431418.1:p.Cys152=
ENST00000674537.1:c.294T>C	ENSP00000502725.1:p.Cys98=
ENST00000358660.3:c.456T>C	ENSP00000351486.3:p.Cys152=
ENST00000368196.7:c.456T>C	ENSP00000357179.3:p.Cys152=
ENST00000392302.6:c.366T>C	ENSP00000376120.2:p.Cys122=
ENST00000489021.6:n.313-5502T>C
ENST00000497019.6:c.366T>C	ENSP00000436804.1:p.Cys122=
ENST00000524377.5:c.456T>C	ENSP00000431418.1:p.Cys152=
ENST00000530298.5:n.514T>C
NM_001007792.1:c.366T>C , LRG_261t1:c.366T>C	NP_001007793.1:p.Cys122=
NM_001012331.1:c.456T>C , LRG_261t2:c.456T>C	NP_001012331.1:p.Cys152=
NM_002529.3:c.456T>C , LRG_261t3:c.456T>C	NP_002520.2:p.Cys152=
NM_001012331.2:c.456T>C	NP_001012331.1:p.Cys152=
NM_002529.4:c.456T>C MANE Select	NP_002520.2:p.Cys152=