Canonical Allele Identifier: CA421271682

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 1971252
• ClinVar RCV Id: RCV002740588
• dbSNP Id: rs2102924257
• gnomAD v4: 1-156879164-T-C
• MyVariant Identifiers: chr1:g.156848956T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879164T>C , CM000663.2:g.156879164T>C	GRCh38
NC_000001.10:g.156848956T>C , CM000663.1:g.156848956T>C	GRCh37
NC_000001.9:g.155115580T>C	NCBI36
NG_007493.1:g.68415T>C , LRG_261:g.68415T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1668T>C	ENSP00000502725.1:p.Asp556=
ENST00000392302.7:c.1668T>C	ENSP00000376120.3:p.Asp556=
ENST00000497019.7:c.*440T>C	ENSP00000436804.2:n.*440T>C
ENST00000524377.7:c.1848T>C MANE Select	ENSP00000431418.1:p.Asp616=
ENST00000674537.1:c.1668T>C	ENSP00000502725.1:p.Asp556=
ENST00000358660.3:c.1839T>C	ENSP00000351486.3:p.Asp613=
ENST00000368196.7:c.1830T>C	ENSP00000357179.3:p.Asp610=
ENST00000392302.6:c.1740T>C	ENSP00000376120.2:p.Asp580=
ENST00000497019.6:c.*440T>C	ENSP00000436804.1:n.*440T>C
ENST00000524377.5:c.1848T>C	ENSP00000431418.1:p.Asp616=
ENST00000530298.5:n.2301T>C
NM_001007792.1:c.1740T>C , LRG_261t1:c.1740T>C	NP_001007793.1:p.Asp580=
NM_001012331.1:c.1830T>C , LRG_261t2:c.1830T>C	NP_001012331.1:p.Asp610=
NM_002529.3:c.1848T>C , LRG_261t3:c.1848T>C	NP_002520.2:p.Asp616=
NM_001012331.2:c.1830T>C	NP_001012331.1:p.Asp610=
NM_002529.4:c.1848T>C MANE Select	NP_002520.2:p.Asp616=