Canonical Allele Identifier: CA889790057

Gene: NTRK1

Linked Data

• dbSNP Id: rs1162323666
• MyVariant Identifiers: chr1:g.156846219_156846230del (hg19) ; chr1:g.156876427_156876438del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876428_156876439del , CM000663.2:g.156876428_156876439del	GRCh38
NC_000001.10:g.156846220_156846231del , CM000663.1:g.156846220_156846231del	GRCh37
NC_000001.9:g.155112844_155112855del	NCBI36
NG_007493.1:g.65679_65690del , LRG_261:g.65679_65690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1481_1492del	ENSP00000502725.1:p.Arg494_Phe497del
ENST00000392302.7:c.1481_1492del	ENSP00000376120.3:p.Arg494_Phe497del
ENST00000497019.7:c.*253_*264del	ENSP00000436804.2:n.*253_*264del
ENST00000524377.7:c.1661_1672del MANE Select	ENSP00000431418.1:p.Arg554_Phe557del
ENST00000674537.1:c.1481_1492del	ENSP00000502725.1:p.Arg494_Phe497del
ENST00000358660.3:c.1652_1663del	ENSP00000351486.3:p.Arg551_Phe554del
ENST00000368196.7:c.1643_1654del	ENSP00000357179.3:p.Arg548_Phe551del
ENST00000392302.6:c.1553_1564del	ENSP00000376120.2:p.Arg518_Phe521del
ENST00000497019.6:c.*253_*264del	ENSP00000436804.1:n.*253_*264del
ENST00000524377.5:c.1661_1672del	ENSP00000431418.1:p.Arg554_Phe557del
ENST00000530298.5:n.2114_2125del
NM_001007792.1:c.1553_1564del , LRG_261t1:c.1553_1564del	NP_001007793.1:p.Arg518_Phe521del
NM_001012331.1:c.1643_1654del , LRG_261t2:c.1643_1654del	NP_001012331.1:p.Arg548_Phe551del
NM_002529.3:c.1661_1672del , LRG_261t3:c.1661_1672del	NP_002520.2:p.Arg554_Phe557del
NM_001012331.2:c.1643_1654del	NP_001012331.1:p.Arg548_Phe551del
NM_002529.4:c.1661_1672del MANE Select	NP_002520.2:p.Arg554_Phe557del