Canonical Allele Identifier: CA421140671

Gene: NTRK1

Linked Data

• dbSNP Id: rs537948663
• gnomAD v4: 1-156881589-C-A
• MyVariant Identifiers: chr1:g.156851381C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881589C>A , CM000663.2:g.156881589C>A	GRCh38
NC_000001.10:g.156851381C>A , CM000663.1:g.156851381C>A	GRCh37
NC_000001.9:g.155118005C>A	NCBI36
NG_007493.1:g.70840C>A , LRG_261:g.70840C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2158C>A	ENSP00000502725.1:p.Arg720=
ENST00000392302.7:c.2158C>A	ENSP00000376120.3:p.Arg720=
ENST00000497019.7:c.*930C>A	ENSP00000436804.2:n.*930C>A
ENST00000524377.7:c.2338C>A MANE Select	ENSP00000431418.1:p.Arg780=
ENST00000531606.2:c.397C>A
ENST00000674537.1:c.2158C>A	ENSP00000502725.1:p.Arg720=
ENST00000358660.3:c.2329C>A	ENSP00000351486.3:p.Arg777=
ENST00000368196.7:c.2320C>A	ENSP00000357179.3:p.Arg774=
ENST00000392302.6:c.2230C>A	ENSP00000376120.2:p.Arg744=
ENST00000497019.6:c.*930C>A	ENSP00000436804.1:n.*930C>A
ENST00000524377.5:c.2338C>A	ENSP00000431418.1:p.Arg780=
ENST00000530298.5:n.2791C>A
ENST00000531606.1:n.381C>A
NM_001007792.1:c.2230C>A , LRG_261t1:c.2230C>A	NP_001007793.1:p.Arg744=
NM_001012331.1:c.2320C>A , LRG_261t2:c.2320C>A	NP_001012331.1:p.Arg774=
NM_002529.3:c.2338C>A , LRG_261t3:c.2338C>A	NP_002520.2:p.Arg780=
NM_001012331.2:c.2320C>A	NP_001012331.1:p.Arg774=
NM_002529.4:c.2338C>A MANE Select	NP_002520.2:p.Arg780=