Canonical Allele Identifier: CA31117614

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 1146142
• ClinVar RCV Id: RCV001485302 ; RCV002562701
• dbSNP Id: rs981404213
• gnomAD v4: 1-156875516-C-G
• MyVariant Identifiers: chr1:g.156845308C>G (hg19) ; chr1:g.156875516C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875516C>G , CM000663.2:g.156875516C>G	GRCh38
NC_000001.10:g.156845308C>G , CM000663.1:g.156845308C>G	GRCh37
NC_000001.9:g.155111932C>G	NCBI36
NG_007493.1:g.64767C>G , LRG_261:g.64767C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1175-4C>G	ENSP00000502725.1:n.1175-4C>G
ENST00000392302.7:c.1175-4C>G	ENSP00000376120.3:n.1175-4C>G
ENST00000497019.7:c.1042-4C>G	ENSP00000436804.2:n.1042-4C>G
ENST00000524377.7:c.1355-4C>G MANE Select	ENSP00000431418.1:n.1355-4C>G
ENST00000674537.1:c.1175-4C>G	ENSP00000502725.1:n.1175-4C>G
ENST00000358660.3:c.1337-4C>G	ENSP00000351486.3:n.1337-4C>G
ENST00000368196.7:c.1337-4C>G	ENSP00000357179.3:n.1337-4C>G
ENST00000392302.6:c.1247-4C>G	ENSP00000376120.2:n.1247-4C>G
ENST00000497019.6:c.1114-4C>G	ENSP00000436804.1:n.1114-4C>G
ENST00000524377.5:c.1355-4C>G	ENSP00000431418.1:n.1355-4C>G
ENST00000530298.5:n.1395-4C>G
ENST00000534682.1:n.578-4C>G
NM_001007792.1:c.1247-4C>G , LRG_261t1:c.1247-4C>G	NP_001007793.1:n.1247-4C>G
NM_001012331.1:c.1337-4C>G , LRG_261t2:c.1337-4C>G	NP_001012331.1:n.1337-4C>G
NM_002529.3:c.1355-4C>G , LRG_261t3:c.1355-4C>G	NP_002520.2:n.1355-4C>G
NM_001012331.2:c.1337-4C>G	NP_001012331.1:n.1337-4C>G
NM_002529.4:c.1355-4C>G MANE Select	NP_002520.2:n.1355-4C>G