Canonical Allele Identifier: CA31116266

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156874560T>C , CM000663.2:g.156874560T>C	GRCh38
NC_000001.10:g.156844352T>C , CM000663.1:g.156844352T>C	GRCh37
NC_000001.9:g.155110976T>C	NCBI36
NG_007493.1:g.63811T>C , LRG_261:g.63811T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1196-11T>C MANE Select	NP_002520.2:n.1196-11T>C
ENST00000524377.7:c.1196-11T>C MANE Select	ENSP00000431418.1:n.1196-11T>C
NM_001007792.1:c.1088-11T>C , LRG_261t1:c.1088-11T>C	NP_001007793.1:n.1088-11T>C
NM_001012331.1:c.1178-11T>C , LRG_261t2:c.1178-11T>C	NP_001012331.1:n.1178-11T>C
NM_001012331.2:c.1178-11T>C	NP_001012331.1:n.1178-11T>C
NM_002529.3:c.1196-11T>C , LRG_261t3:c.1196-11T>C	NP_002520.2:n.1196-11T>C
ENST00000358660.3:c.1178-11T>C	ENSP00000351486.3:n.1178-11T>C
ENST00000368196.7:c.1178-11T>C	ENSP00000357179.3:n.1178-11T>C
ENST00000392302.6:c.1088-11T>C	ENSP00000376120.2:n.1088-11T>C
ENST00000392302.7:c.1016-11T>C	ENSP00000376120.3:n.1016-11T>C
ENST00000497019.6:c.955-11T>C	ENSP00000436804.1:n.955-11T>C
ENST00000497019.7:c.883-11T>C	ENSP00000436804.2:n.883-11T>C
ENST00000524377.5:c.1196-11T>C	ENSP00000431418.1:n.1196-11T>C
ENST00000530298.5:n.1236-11T>C
ENST00000534682.1:n.408T>C
ENST00000674537.1:c.1016-11T>C	ENSP00000502725.1:n.1016-11T>C
ENST00000674537.2:c.1016-11T>C	ENSP00000502725.1:n.1016-11T>C