Canonical Allele Identifier: CA1169251

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156874612G>C , CM000663.2:g.156874612G>C	GRCh38
NC_000001.10:g.156844404G>C , CM000663.1:g.156844404G>C	GRCh37
NC_000001.9:g.155111028G>C	NCBI36
NG_007493.1:g.63863G>C , LRG_261:g.63863G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1237G>C MANE Select	NP_002520.2:p.Glu413Gln
ENST00000524377.7:c.1237G>C MANE Select	ENSP00000431418.1:p.Glu413Gln
NM_001007792.1:c.1129G>C , LRG_261t1:c.1129G>C	NP_001007793.1:p.Glu377Gln
NM_001012331.1:c.1219G>C , LRG_261t2:c.1219G>C	NP_001012331.1:p.Glu407Gln
NM_001012331.2:c.1219G>C	NP_001012331.1:p.Glu407Gln
NM_002529.3:c.1237G>C , LRG_261t3:c.1237G>C	NP_002520.2:p.Glu413Gln
ENST00000358660.3:c.1219G>C	ENSP00000351486.3:p.Glu407Gln
ENST00000368196.7:c.1219G>C	ENSP00000357179.3:p.Glu407Gln
ENST00000392302.6:c.1129G>C	ENSP00000376120.2:p.Glu377Gln
ENST00000392302.7:c.1057G>C	ENSP00000376120.3:p.Glu353Gln
ENST00000497019.6:c.996G>C	ENSP00000436804.1:p.Thr332=
ENST00000497019.7:c.924G>C	ENSP00000436804.2:p.Thr308=
ENST00000524377.5:c.1237G>C	ENSP00000431418.1:p.Glu413Gln
ENST00000530298.5:n.1277G>C
ENST00000534682.1:n.460G>C
ENST00000674537.1:c.1057G>C	ENSP00000502725.1:p.Glu353Gln
ENST00000674537.2:c.1057G>C	ENSP00000502725.1:p.Glu353Gln