Canonical Allele Identifier: CA2648463768

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102918255
• gnomAD v4: 1-156876265-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876265C>T , CM000663.2:g.156876265C>T	GRCh38
NC_000001.10:g.156846057C>T , CM000663.1:g.156846057C>T	GRCh37
NC_000001.9:g.155112681C>T	NCBI36
NG_007493.1:g.65516C>T , LRG_261:g.65516C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1452+55C>T	ENSP00000502725.1:n.1452+55C>T
ENST00000392302.7:c.1452+55C>T	ENSP00000376120.3:n.1452+55C>T
ENST00000497019.7:c.*224+55C>T	ENSP00000436804.2:n.*224+55C>T
ENST00000524377.7:c.1632+55C>T MANE Select	ENSP00000431418.1:n.1632+55C>T
ENST00000674537.1:c.1452+55C>T	ENSP00000502725.1:n.1452+55C>T
ENST00000358660.3:c.1623+55C>T	ENSP00000351486.3:n.1623+55C>T
ENST00000368196.7:c.1614+55C>T	ENSP00000357179.3:n.1614+55C>T
ENST00000392302.6:c.1524+55C>T	ENSP00000376120.2:n.1524+55C>T
ENST00000497019.6:c.*224+55C>T	ENSP00000436804.1:n.*224+55C>T
ENST00000524377.5:c.1632+55C>T	ENSP00000431418.1:n.1632+55C>T
ENST00000530298.5:n.2085+55C>T
NM_001007792.1:c.1524+55C>T , LRG_261t1:c.1524+55C>T	NP_001007793.1:n.1524+55C>T
NM_001012331.1:c.1614+55C>T , LRG_261t2:c.1614+55C>T	NP_001012331.1:n.1614+55C>T
NM_002529.3:c.1632+55C>T , LRG_261t3:c.1632+55C>T	NP_002520.2:n.1632+55C>T
NM_001012331.2:c.1614+55C>T	NP_001012331.1:n.1614+55C>T
NM_002529.4:c.1632+55C>T MANE Select	NP_002520.2:n.1632+55C>T