Canonical Allele Identifier: CA342941416

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 1026216
• ClinVar RCV Id: RCV001326638
• dbSNP Id: rs1444452580
• gnomAD v2: 1-156851277-A-G
• gnomAD v4: 1-156881485-A-G
• MyVariant Identifiers: chr1:g.156851277A>G (hg19) ; chr1:g.156881485A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881485A>G , CM000663.2:g.156881485A>G	GRCh38
NC_000001.10:g.156851277A>G , CM000663.1:g.156851277A>G	GRCh37
NC_000001.9:g.155117901A>G	NCBI36
NG_007493.1:g.70736A>G , LRG_261:g.70736A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.2054A>G	ENSP00000502725.1:p.Glu685Gly
ENST00000392302.7:c.2054A>G	ENSP00000376120.3:p.Glu685Gly
ENST00000497019.7:c.*826A>G	ENSP00000436804.2:n.*826A>G
ENST00000524377.7:c.2234A>G MANE Select	ENSP00000431418.1:p.Glu745Gly
ENST00000531606.2:c.293A>G
ENST00000674537.1:c.2054A>G	ENSP00000502725.1:p.Glu685Gly
ENST00000358660.3:c.2225A>G	ENSP00000351486.3:p.Glu742Gly
ENST00000368196.7:c.2216A>G	ENSP00000357179.3:p.Glu739Gly
ENST00000392302.6:c.2126A>G	ENSP00000376120.2:p.Glu709Gly
ENST00000497019.6:c.*826A>G	ENSP00000436804.1:n.*826A>G
ENST00000524377.5:c.2234A>G	ENSP00000431418.1:p.Glu745Gly
ENST00000530298.5:n.2687A>G
ENST00000531606.1:n.277A>G
NM_001007792.1:c.2126A>G , LRG_261t1:c.2126A>G	NP_001007793.1:p.Glu709Gly
NM_001012331.1:c.2216A>G , LRG_261t2:c.2216A>G	NP_001012331.1:p.Glu739Gly
NM_002529.3:c.2234A>G , LRG_261t3:c.2234A>G	NP_002520.2:p.Glu745Gly
NM_001012331.2:c.2216A>G	NP_001012331.1:p.Glu739Gly
NM_002529.4:c.2234A>G MANE Select	NP_002520.2:p.Glu745Gly