Canonical Allele Identifier: CA342941478

Gene: NTRK1

Linked Data

• dbSNP Id: rs1009726086
• gnomAD v4: 1-156881499-C-A
• MyVariant Identifiers: chr1:g.156851291C>A (hg19) ; chr1:g.156881499C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881499C>A , CM000663.2:g.156881499C>A	GRCh38
NC_000001.10:g.156851291C>A , CM000663.1:g.156851291C>A	GRCh37
NC_000001.9:g.155117915C>A	NCBI36
NG_007493.1:g.70750C>A , LRG_261:g.70750C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2068C>A	ENSP00000502725.1:p.Arg690Ser
ENST00000392302.7:c.2068C>A	ENSP00000376120.3:p.Arg690Ser
ENST00000497019.7:c.*840C>A	ENSP00000436804.2:n.*840C>A
ENST00000524377.7:c.2248C>A MANE Select	ENSP00000431418.1:p.Arg750Ser
ENST00000531606.2:c.307C>A
ENST00000674537.1:c.2068C>A	ENSP00000502725.1:p.Arg690Ser
ENST00000358660.3:c.2239C>A	ENSP00000351486.3:p.Arg747Ser
ENST00000368196.7:c.2230C>A	ENSP00000357179.3:p.Arg744Ser
ENST00000392302.6:c.2140C>A	ENSP00000376120.2:p.Arg714Ser
ENST00000497019.6:c.*840C>A	ENSP00000436804.1:n.*840C>A
ENST00000524377.5:c.2248C>A	ENSP00000431418.1:p.Arg750Ser
ENST00000530298.5:n.2701C>A
ENST00000531606.1:n.291C>A
NM_001007792.1:c.2140C>A , LRG_261t1:c.2140C>A	NP_001007793.1:p.Arg714Ser
NM_001012331.1:c.2230C>A , LRG_261t2:c.2230C>A	NP_001012331.1:p.Arg744Ser
NM_002529.3:c.2248C>A , LRG_261t3:c.2248C>A	NP_002520.2:p.Arg750Ser
NM_001012331.2:c.2230C>A	NP_001012331.1:p.Arg744Ser
NM_002529.4:c.2248C>A MANE Select	NP_002520.2:p.Arg750Ser