Canonical Allele Identifier: CA342941763

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156881605-C-T
• MyVariant Identifiers: chr1:g.156851397C>T (hg19) ; chr1:g.156881605C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881605C>T , CM000663.2:g.156881605C>T	GRCh38
NC_000001.10:g.156851397C>T , CM000663.1:g.156851397C>T	GRCh37
NC_000001.9:g.155118021C>T	NCBI36
NG_007493.1:g.70856C>T , LRG_261:g.70856C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2174C>T	ENSP00000502725.1:p.Ala725Val
ENST00000392302.7:c.2174C>T	ENSP00000376120.3:p.Ala725Val
ENST00000497019.7:c.*946C>T	ENSP00000436804.2:n.*946C>T
ENST00000524377.7:c.2354C>T MANE Select	ENSP00000431418.1:p.Ala785Val
ENST00000531606.2:c.413C>T
ENST00000674537.1:c.2174C>T	ENSP00000502725.1:p.Ala725Val
ENST00000358660.3:c.2345C>T	ENSP00000351486.3:p.Ala782Val
ENST00000368196.7:c.2336C>T	ENSP00000357179.3:p.Ala779Val
ENST00000392302.6:c.2246C>T	ENSP00000376120.2:p.Ala749Val
ENST00000497019.6:c.*946C>T	ENSP00000436804.1:n.*946C>T
ENST00000524377.5:c.2354C>T	ENSP00000431418.1:p.Ala785Val
ENST00000530298.5:n.2807C>T
ENST00000531606.1:n.397C>T
NM_001007792.1:c.2246C>T , LRG_261t1:c.2246C>T	NP_001007793.1:p.Ala749Val
NM_001012331.1:c.2336C>T , LRG_261t2:c.2336C>T	NP_001012331.1:p.Ala779Val
NM_002529.3:c.2354C>T , LRG_261t3:c.2354C>T	NP_002520.2:p.Ala785Val
NM_001012331.2:c.2336C>T	NP_001012331.1:p.Ala779Val
NM_002529.4:c.2354C>T MANE Select	NP_002520.2:p.Ala785Val