Canonical Allele Identifier: CA342938110

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917650
• gnomAD v4: 1-156876169-A-G
• MyVariant Identifiers: chr1:g.156845961A>G (hg19) ; chr1:g.156876169A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876169A>G , CM000663.2:g.156876169A>G	GRCh38
NC_000001.10:g.156845961A>G , CM000663.1:g.156845961A>G	GRCh37
NC_000001.9:g.155112585A>G	NCBI36
NG_007493.1:g.65420A>G , LRG_261:g.65420A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1411A>G	ENSP00000502725.1:p.Asn471Asp
ENST00000392302.7:c.1411A>G	ENSP00000376120.3:p.Asn471Asp
ENST00000497019.7:c.*183A>G	ENSP00000436804.2:n.*183A>G
ENST00000524377.7:c.1591A>G MANE Select	ENSP00000431418.1:p.Asn531Asp
ENST00000674537.1:c.1411A>G	ENSP00000502725.1:p.Asn471Asp
ENST00000358660.3:c.1582A>G	ENSP00000351486.3:p.Asn528Asp
ENST00000368196.7:c.1573A>G	ENSP00000357179.3:p.Asn525Asp
ENST00000392302.6:c.1483A>G	ENSP00000376120.2:p.Asn495Asp
ENST00000497019.6:c.*183A>G	ENSP00000436804.1:n.*183A>G
ENST00000524377.5:c.1591A>G	ENSP00000431418.1:p.Asn531Asp
ENST00000530298.5:n.2044A>G
ENST00000534682.1:n.814A>G
NM_001007792.1:c.1483A>G , LRG_261t1:c.1483A>G	NP_001007793.1:p.Asn495Asp
NM_001012331.1:c.1573A>G , LRG_261t2:c.1573A>G	NP_001012331.1:p.Asn525Asp
NM_002529.3:c.1591A>G , LRG_261t3:c.1591A>G	NP_002520.2:p.Asn531Asp
NM_001012331.2:c.1573A>G	NP_001012331.1:p.Asn525Asp
NM_002529.4:c.1591A>G MANE Select	NP_002520.2:p.Asn531Asp