Canonical Allele Identifier: CA1200785981

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876251_156876252delinsAC , CM000663.2:g.156876251_156876252delinsAC	GRCh38
NC_000001.10:g.156846043_156846044delinsAC , CM000663.1:g.156846043_156846044delinsAC	GRCh37
NC_000001.9:g.155112667_155112668delinsAC	NCBI36
NG_007493.1:g.65502_65503delinsAC , LRG_261:g.65502_65503delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1452+41_1452+42delinsAC	ENSP00000502725.1:n.1452+41_1452+42delinsAC
ENST00000392302.7:c.1452+41_1452+42delinsAC	ENSP00000376120.3:n.1452+41_1452+42delinsAC
ENST00000497019.7:c.*224+41_*224+42delinsAC	ENSP00000436804.2:n.*224+41_*224+42delinsAC
ENST00000524377.7:c.1632+41_1632+42delinsAC MANE Select	ENSP00000431418.1:n.1632+41_1632+42delinsAC
ENST00000674537.1:c.1452+41_1452+42delinsAC	ENSP00000502725.1:n.1452+41_1452+42delinsAC
ENST00000358660.3:c.1623+41_1623+42delinsAC	ENSP00000351486.3:n.1623+41_1623+42delinsAC
ENST00000368196.7:c.1614+41_1614+42delinsAC	ENSP00000357179.3:n.1614+41_1614+42delinsAC
ENST00000392302.6:c.1524+41_1524+42delinsAC	ENSP00000376120.2:n.1524+41_1524+42delinsAC
ENST00000497019.6:c.*224+41_*224+42delinsAC	ENSP00000436804.1:n.*224+41_*224+42delinsAC
ENST00000524377.5:c.1632+41_1632+42delinsAC	ENSP00000431418.1:n.1632+41_1632+42delinsAC
ENST00000530298.5:n.2085+41_2085+42delinsAC
NM_001007792.1:c.1524+41_1524+42delinsAC , LRG_261t1:c.1524+41_1524+42delinsAC	NP_001007793.1:n.1524+41_1524+42delinsAC
NM_001012331.1:c.1614+41_1614+42delinsAC , LRG_261t2:c.1614+41_1614+42delinsAC	NP_001012331.1:n.1614+41_1614+42delinsAC
NM_002529.3:c.1632+41_1632+42delinsAC , LRG_261t3:c.1632+41_1632+42delinsAC	NP_002520.2:n.1632+41_1632+42delinsAC
NM_001012331.2:c.1614+41_1614+42delinsAC	NP_001012331.1:n.1614+41_1614+42delinsAC
NM_002529.4:c.1632+41_1632+42delinsAC MANE Select	NP_002520.2:n.1632+41_1632+42delinsAC