Canonical Allele Identifier: CA342938163

Gene: NTRK1

Linked Data

• dbSNP Id: rs1395947150
• MyVariant Identifiers: chr1:g.156845974A>T (hg19) ; chr1:g.156876182A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876182A>T , CM000663.2:g.156876182A>T	GRCh38
NC_000001.10:g.156845974A>T , CM000663.1:g.156845974A>T	GRCh37
NC_000001.9:g.155112598A>T	NCBI36
NG_007493.1:g.65433A>T , LRG_261:g.65433A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1424A>T	ENSP00000502725.1:p.Glu475Val
ENST00000392302.7:c.1424A>T	ENSP00000376120.3:p.Glu475Val
ENST00000497019.7:c.*196A>T	ENSP00000436804.2:n.*196A>T
ENST00000524377.7:c.1604A>T MANE Select	ENSP00000431418.1:p.Glu535Val
ENST00000674537.1:c.1424A>T	ENSP00000502725.1:p.Glu475Val
ENST00000358660.3:c.1595A>T	ENSP00000351486.3:p.Glu532Val
ENST00000368196.7:c.1586A>T	ENSP00000357179.3:p.Glu529Val
ENST00000392302.6:c.1496A>T	ENSP00000376120.2:p.Glu499Val
ENST00000497019.6:c.*196A>T	ENSP00000436804.1:n.*196A>T
ENST00000524377.5:c.1604A>T	ENSP00000431418.1:p.Glu535Val
ENST00000530298.5:n.2057A>T
ENST00000534682.1:n.827A>T
NM_001007792.1:c.1496A>T , LRG_261t1:c.1496A>T	NP_001007793.1:p.Glu499Val
NM_001012331.1:c.1586A>T , LRG_261t2:c.1586A>T	NP_001012331.1:p.Glu529Val
NM_002529.3:c.1604A>T , LRG_261t3:c.1604A>T	NP_002520.2:p.Glu535Val
NM_001012331.2:c.1586A>T	NP_001012331.1:p.Glu529Val
NM_002529.4:c.1604A>T MANE Select	NP_002520.2:p.Glu535Val