Canonical Allele Identifier: CA342936136

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156873858A>C , CM000663.2:g.156873858A>C	GRCh38
NC_000001.10:g.156843650A>C , CM000663.1:g.156843650A>C	GRCh37
NC_000001.9:g.155110274A>C	NCBI36
NG_007493.1:g.63109A>C , LRG_261:g.63109A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.914A>C	ENSP00000502725.1:p.Tyr305Ser
ENST00000392302.7:c.914A>C	ENSP00000376120.3:p.Tyr305Ser
ENST00000497019.7:c.781A>C	ENSP00000436804.2:p.Thr261Pro
ENST00000524377.7:c.1076A>C MANE Select	ENSP00000431418.1:p.Tyr359Ser
ENST00000674537.1:c.914A>C	ENSP00000502725.1:p.Tyr305Ser
ENST00000358660.3:c.1076A>C	ENSP00000351486.3:p.Tyr359Ser
ENST00000368196.7:c.1076A>C	ENSP00000357179.3:p.Tyr359Ser
ENST00000392302.6:c.986A>C	ENSP00000376120.2:p.Tyr329Ser
ENST00000489021.6:n.538A>C
ENST00000497019.6:c.853A>C	ENSP00000436804.1:p.Thr285Pro
ENST00000524377.5:c.1076A>C	ENSP00000431418.1:p.Tyr359Ser
ENST00000530298.5:n.1134A>C
NM_001007792.1:c.986A>C , LRG_261t1:c.986A>C	NP_001007793.1:p.Tyr329Ser
NM_001012331.1:c.1076A>C , LRG_261t2:c.1076A>C	NP_001012331.1:p.Tyr359Ser
NM_002529.3:c.1076A>C , LRG_261t3:c.1076A>C	NP_002520.2:p.Tyr359Ser
NM_001012331.2:c.1076A>C	NP_001012331.1:p.Tyr359Ser
NM_002529.4:c.1076A>C MANE Select	NP_002520.2:p.Tyr359Ser