Canonical Allele Identifier: CA2648462738

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156868034-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156868034G>T , CM000663.2:g.156868034G>T	GRCh38
NC_000001.10:g.156837826G>T , CM000663.1:g.156837826G>T	GRCh37
NC_000001.9:g.155104450G>T	NCBI36
NG_007493.1:g.57285G>T , LRG_261:g.57285G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.267-70G>T	ENSP00000502725.1:n.267-70G>T
ENST00000392302.7:c.267-70G>T	ENSP00000376120.3:n.267-70G>T
ENST00000497019.7:c.267-70G>T	ENSP00000436804.2:n.267-70G>T
ENST00000524377.7:c.429-70G>T MANE Select	ENSP00000431418.1:n.429-70G>T
ENST00000674537.1:c.267-70G>T	ENSP00000502725.1:n.267-70G>T
ENST00000358660.3:c.429-70G>T	ENSP00000351486.3:n.429-70G>T
ENST00000368196.7:c.429-70G>T	ENSP00000357179.3:n.429-70G>T
ENST00000392302.6:c.339-70G>T	ENSP00000376120.2:n.339-70G>T
ENST00000489021.6:n.313-5599G>T
ENST00000497019.6:c.339-70G>T	ENSP00000436804.1:n.339-70G>T
ENST00000524377.5:c.429-70G>T	ENSP00000431418.1:n.429-70G>T
ENST00000530298.5:n.487-70G>T
NM_001007792.1:c.339-70G>T , LRG_261t1:c.339-70G>T	NP_001007793.1:n.339-70G>T
NM_001012331.1:c.429-70G>T , LRG_261t2:c.429-70G>T	NP_001012331.1:n.429-70G>T
NM_002529.3:c.429-70G>T , LRG_261t3:c.429-70G>T	NP_002520.2:n.429-70G>T
NM_001012331.2:c.429-70G>T	NP_001012331.1:n.429-70G>T
NM_002529.4:c.429-70G>T MANE Select	NP_002520.2:n.429-70G>T