Canonical Allele Identifier: CA2648463789

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156876283-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876289dup , CM000663.2:g.156876289dup	GRCh38
NC_000001.10:g.156846081dup , CM000663.1:g.156846081dup	GRCh37
NC_000001.9:g.155112705dup	NCBI36
NG_007493.1:g.65540dup , LRG_261:g.65540dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1452+79dup	ENSP00000502725.1:n.1452+79dup
ENST00000392302.7:c.1452+79dup	ENSP00000376120.3:n.1452+79dup
ENST00000497019.7:c.*224+79dup	ENSP00000436804.2:n.*224+79dup
ENST00000524377.7:c.1632+79dup MANE Select	ENSP00000431418.1:n.1632+79dup
ENST00000674537.1:c.1452+79dup	ENSP00000502725.1:n.1452+79dup
ENST00000358660.3:c.1623+79dup	ENSP00000351486.3:n.1623+79dup
ENST00000368196.7:c.1614+79dup	ENSP00000357179.3:n.1614+79dup
ENST00000392302.6:c.1524+79dup	ENSP00000376120.2:n.1524+79dup
ENST00000497019.6:c.*224+79dup	ENSP00000436804.1:n.*224+79dup
ENST00000524377.5:c.1632+79dup	ENSP00000431418.1:n.1632+79dup
ENST00000530298.5:n.2085+79dup
NM_001007792.1:c.1524+79dup , LRG_261t1:c.1524+79dup	NP_001007793.1:n.1524+79dup
NM_001012331.1:c.1614+79dup , LRG_261t2:c.1614+79dup	NP_001012331.1:n.1614+79dup
NM_002529.3:c.1632+79dup , LRG_261t3:c.1632+79dup	NP_002520.2:n.1632+79dup
NM_001012331.2:c.1614+79dup	NP_001012331.1:n.1614+79dup
NM_002529.4:c.1632+79dup MANE Select	NP_002520.2:n.1632+79dup