Canonical Allele Identifier: CA1168867

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156864394C>A , CM000663.2:g.156864394C>A	GRCh38
NC_000001.10:g.156834186C>A , CM000663.1:g.156834186C>A	GRCh37
NC_000001.9:g.155100810C>A	NCBI36
NG_007493.1:g.53645C>A , LRG_261:g.53645C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.253C>A MANE Select	NP_002520.2:p.Arg85Ser
ENST00000524377.7:c.253C>A MANE Select	ENSP00000431418.1:p.Arg85Ser
NM_001007792.1:c.163C>A , LRG_261t1:c.163C>A	NP_001007793.1:p.Arg55Ser
NM_001012331.1:c.253C>A , LRG_261t2:c.253C>A	NP_001012331.1:p.Arg85Ser
NM_001012331.2:c.253C>A	NP_001012331.1:p.Arg85Ser
NM_002529.3:c.253C>A , LRG_261t3:c.253C>A	NP_002520.2:p.Arg85Ser
ENST00000358660.3:c.253C>A	ENSP00000351486.3:p.Arg85Ser
ENST00000368196.7:c.253C>A	ENSP00000357179.3:p.Arg85Ser
ENST00000392302.6:c.163C>A	ENSP00000376120.2:p.Arg55Ser
ENST00000392302.7:c.91C>A	ENSP00000376120.3:p.Arg31Ser
ENST00000489021.6:n.313-9239C>A
ENST00000497019.6:c.163C>A	ENSP00000436804.1:p.Arg55Ser
ENST00000497019.7:c.91C>A	ENSP00000436804.2:p.Arg31Ser
ENST00000524377.5:c.253C>A	ENSP00000431418.1:p.Arg85Ser
ENST00000530298.5:n.311C>A
ENST00000533630.1:n.275C>A
ENST00000674537.1:c.91C>A	ENSP00000502725.1:p.Arg31Ser
ENST00000674537.2:c.91C>A	ENSP00000502725.1:p.Arg31Ser
ENST00000675461.1:c.253C>A	ENSP00000501668.1:p.Arg85Ser