Canonical Allele Identifier: CA342937882

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917310
• gnomAD v3: 1-156876112-C-T
• gnomAD v4: 1-156876112-C-T
• MyVariant Identifiers: chr1:g.156845904C>T (hg19) ; chr1:g.156876112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876112C>T , CM000663.2:g.156876112C>T	GRCh38
NC_000001.10:g.156845904C>T , CM000663.1:g.156845904C>T	GRCh37
NC_000001.9:g.155112528C>T	NCBI36
NG_007493.1:g.65363C>T , LRG_261:g.65363C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1354C>T	ENSP00000502725.1:p.Leu452Phe
ENST00000392302.7:c.1354C>T	ENSP00000376120.3:p.Leu452Phe
ENST00000497019.7:c.*126C>T	ENSP00000436804.2:n.*126C>T
ENST00000524377.7:c.1534C>T MANE Select	ENSP00000431418.1:p.Leu512Phe
ENST00000674537.1:c.1354C>T	ENSP00000502725.1:p.Leu452Phe
ENST00000358660.3:c.1525C>T	ENSP00000351486.3:p.Leu509Phe
ENST00000368196.7:c.1516C>T	ENSP00000357179.3:p.Leu506Phe
ENST00000392302.6:c.1426C>T	ENSP00000376120.2:p.Leu476Phe
ENST00000497019.6:c.*126C>T	ENSP00000436804.1:n.*126C>T
ENST00000524377.5:c.1534C>T	ENSP00000431418.1:p.Leu512Phe
ENST00000530298.5:n.1987C>T
ENST00000534682.1:n.757C>T
NM_001007792.1:c.1426C>T , LRG_261t1:c.1426C>T	NP_001007793.1:p.Leu476Phe
NM_001012331.1:c.1516C>T , LRG_261t2:c.1516C>T	NP_001012331.1:p.Leu506Phe
NM_002529.3:c.1534C>T , LRG_261t3:c.1534C>T	NP_002520.2:p.Leu512Phe
NM_001012331.2:c.1516C>T	NP_001012331.1:p.Leu506Phe
NM_002529.4:c.1534C>T MANE Select	NP_002520.2:p.Leu512Phe