Canonical Allele Identifier: CA342938461

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102919257
• MyVariant Identifiers: chr1:g.156846228T>C (hg19) ; chr1:g.156876436T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876436T>C , CM000663.2:g.156876436T>C	GRCh38
NC_000001.10:g.156846228T>C , CM000663.1:g.156846228T>C	GRCh37
NC_000001.9:g.155112852T>C	NCBI36
NG_007493.1:g.65687T>C , LRG_261:g.65687T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1489T>C	ENSP00000502725.1:p.Phe497Leu
ENST00000392302.7:c.1489T>C	ENSP00000376120.3:p.Phe497Leu
ENST00000497019.7:c.*261T>C	ENSP00000436804.2:n.*261T>C
ENST00000524377.7:c.1669T>C MANE Select	ENSP00000431418.1:p.Phe557Leu
ENST00000674537.1:c.1489T>C	ENSP00000502725.1:p.Phe497Leu
ENST00000358660.3:c.1660T>C	ENSP00000351486.3:p.Phe554Leu
ENST00000368196.7:c.1651T>C	ENSP00000357179.3:p.Phe551Leu
ENST00000392302.6:c.1561T>C	ENSP00000376120.2:p.Phe521Leu
ENST00000497019.6:c.*261T>C	ENSP00000436804.1:n.*261T>C
ENST00000524377.5:c.1669T>C	ENSP00000431418.1:p.Phe557Leu
ENST00000530298.5:n.2122T>C
NM_001007792.1:c.1561T>C , LRG_261t1:c.1561T>C	NP_001007793.1:p.Phe521Leu
NM_001012331.1:c.1651T>C , LRG_261t2:c.1651T>C	NP_001012331.1:p.Phe551Leu
NM_002529.3:c.1669T>C , LRG_261t3:c.1669T>C	NP_002520.2:p.Phe557Leu
NM_001012331.2:c.1651T>C	NP_001012331.1:p.Phe551Leu
NM_002529.4:c.1669T>C MANE Select	NP_002520.2:p.Phe557Leu