Canonical Allele Identifier: CA16603426

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 386756
• ClinVar RCV Id: RCV000441510
• dbSNP Id: rs1057522593
• gnomAD v2: 1-156830683-C-T
• gnomAD v3: 1-156860891-C-T
• gnomAD v4: 1-156860891-C-T
• MyVariant Identifiers: chr1:g.156830683C>T (hg19) ; chr1:g.156860891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860891C>T , CM000663.2:g.156860891C>T	GRCh38
NC_000001.10:g.156830683C>T , CM000663.1:g.156830683C>T	GRCh37
NC_000001.9:g.155097307C>T	NCBI36
NG_007493.1:g.50142C>T , LRG_261:g.50142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3463C>T	ENSP00000502725.1:n.51-3463C>T
ENST00000392302.7:c.51-3463C>T	ENSP00000376120.3:n.51-3463C>T
ENST00000497019.7:c.51-3463C>T	ENSP00000436804.2:n.51-3463C>T
ENST00000524377.7:c.-44C>T MANE Select	ENSP00000431418.1:n.-44C>T
ENST00000674537.1:c.51-3463C>T	ENSP00000502725.1:n.51-3463C>T
ENST00000368196.7:c.-44C>T	ENSP00000357179.3:n.-44C>T
ENST00000392302.6:c.123-3463C>T	ENSP00000376120.2:n.123-3463C>T
ENST00000489021.6:n.313-12742C>T
ENST00000497019.6:c.123-3463C>T	ENSP00000436804.1:n.123-3463C>T
ENST00000530298.5:n.271-3463C>T
NM_001007792.1:c.123-3463C>T , LRG_261t1:c.123-3463C>T	NP_001007793.1:n.123-3463C>T
NM_001012331.1:c.-44C>T , LRG_261t2:c.-44C>T	NP_001012331.1:n.-44C>T
NM_002529.3:c.-44C>T , LRG_261t3:c.-44C>T	NP_002520.2:n.-44C>T
NM_001012331.2:c.-44C>T	NP_001012331.1:n.-44C>T
NM_002529.4:c.-44C>T MANE Select	NP_002520.2:n.-44C>T