Canonical Allele Identifier: CA2648465113

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156860870-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860870C>A , CM000663.2:g.156860870C>A	GRCh38
NC_000001.10:g.156830662C>A , CM000663.1:g.156830662C>A	GRCh37
NC_000001.9:g.155097286C>A	NCBI36
NG_007493.1:g.50121C>A , LRG_261:g.50121C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3484C>A	ENSP00000502725.1:n.51-3484C>A
ENST00000392302.7:c.51-3484C>A	ENSP00000376120.3:n.51-3484C>A
ENST00000497019.7:c.51-3484C>A	ENSP00000436804.2:n.51-3484C>A
ENST00000524377.7:c.-65C>A MANE Select	ENSP00000431418.1:n.-65C>A
ENST00000674537.1:c.51-3484C>A	ENSP00000502725.1:n.51-3484C>A
ENST00000368196.7:c.-65C>A	ENSP00000357179.3:n.-65C>A
ENST00000392302.6:c.123-3484C>A	ENSP00000376120.2:n.123-3484C>A
ENST00000489021.6:n.313-12763C>A
ENST00000497019.6:c.123-3484C>A	ENSP00000436804.1:n.123-3484C>A
ENST00000530298.5:n.271-3484C>A
NM_001007792.1:c.123-3484C>A , LRG_261t1:c.123-3484C>A	NP_001007793.1:n.123-3484C>A
NM_001012331.2:c.-65C>A	NP_001012331.1:n.-65C>A
NM_002529.4:c.-65C>A MANE Select	NP_002520.2:n.-65C>A