Canonical Allele Identifier: CA342941772

Gene: NTRK1

Linked Data

• dbSNP Id: rs775966454
• MyVariant Identifiers: chr1:g.156851401G>T (hg19) ; chr1:g.156881609G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881609G>T , CM000663.2:g.156881609G>T	GRCh38
NC_000001.10:g.156851401G>T , CM000663.1:g.156851401G>T	GRCh37
NC_000001.9:g.155118025G>T	NCBI36
NG_007493.1:g.70860G>T , LRG_261:g.70860G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2178G>T	ENSP00000502725.1:p.Gln726His
ENST00000392302.7:c.2178G>T	ENSP00000376120.3:p.Gln726His
ENST00000497019.7:c.*950G>T	ENSP00000436804.2:n.*950G>T
ENST00000524377.7:c.2358G>T MANE Select	ENSP00000431418.1:p.Gln786His
ENST00000531606.2:c.417G>T
ENST00000674537.1:c.2178G>T	ENSP00000502725.1:p.Gln726His
ENST00000358660.3:c.2349G>T	ENSP00000351486.3:p.Gln783His
ENST00000368196.7:c.2340G>T	ENSP00000357179.3:p.Gln780His
ENST00000392302.6:c.2250G>T	ENSP00000376120.2:p.Gln750His
ENST00000497019.6:c.*950G>T	ENSP00000436804.1:n.*950G>T
ENST00000524377.5:c.2358G>T	ENSP00000431418.1:p.Gln786His
ENST00000530298.5:n.2811G>T
ENST00000531606.1:n.401G>T
NM_001007792.1:c.2250G>T , LRG_261t1:c.2250G>T	NP_001007793.1:p.Gln750His
NM_001012331.1:c.2340G>T , LRG_261t2:c.2340G>T	NP_001012331.1:p.Gln780His
NM_002529.3:c.2358G>T , LRG_261t3:c.2358G>T	NP_002520.2:p.Gln786His
NM_001012331.2:c.2340G>T	NP_001012331.1:p.Gln780His
NM_002529.4:c.2358G>T MANE Select	NP_002520.2:p.Gln786His