Canonical Allele Identifier: CA1200787203

Gene: NTRK1

Linked Data

• dbSNP Id: rs748579821
• gnomAD v4: 1-156879083-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879083A>C , CM000663.2:g.156879083A>C	GRCh38
NC_000001.10:g.156848875A>C , CM000663.1:g.156848875A>C	GRCh37
NC_000001.9:g.155115499A>C	NCBI36
NG_007493.1:g.68334A>C , LRG_261:g.68334A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1626-39A>C	ENSP00000502725.1:n.1626-39A>C
ENST00000392302.7:c.1626-39A>C	ENSP00000376120.3:n.1626-39A>C
ENST00000497019.7:c.*398-39A>C	ENSP00000436804.2:n.*398-39A>C
ENST00000524377.7:c.1806-39A>C MANE Select	ENSP00000431418.1:n.1806-39A>C
ENST00000674537.1:c.1626-39A>C	ENSP00000502725.1:n.1626-39A>C
ENST00000358660.3:c.1797-39A>C	ENSP00000351486.3:n.1797-39A>C
ENST00000368196.7:c.1788-39A>C	ENSP00000357179.3:n.1788-39A>C
ENST00000392302.6:c.1698-39A>C	ENSP00000376120.2:n.1698-39A>C
ENST00000497019.6:c.*398-39A>C	ENSP00000436804.1:n.*398-39A>C
ENST00000524377.5:c.1806-39A>C	ENSP00000431418.1:n.1806-39A>C
ENST00000530298.5:n.2259-39A>C
NM_001007792.1:c.1698-39A>C , LRG_261t1:c.1698-39A>C	NP_001007793.1:n.1698-39A>C
NM_001012331.1:c.1788-39A>C , LRG_261t2:c.1788-39A>C	NP_001012331.1:n.1788-39A>C
NM_002529.3:c.1806-39A>C , LRG_261t3:c.1806-39A>C	NP_002520.2:n.1806-39A>C
NM_001012331.2:c.1788-39A>C	NP_001012331.1:n.1788-39A>C
NM_002529.4:c.1806-39A>C MANE Select	NP_002520.2:n.1806-39A>C