Canonical Allele Identifier: CA342940259

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102927146
• MyVariant Identifiers: chr1:g.156849813C>G (hg19) ; chr1:g.156880021C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880021C>G , CM000663.2:g.156880021C>G	GRCh38
NC_000001.10:g.156849813C>G , CM000663.1:g.156849813C>G	GRCh37
NC_000001.9:g.155116437C>G	NCBI36
NG_007493.1:g.69272C>G , LRG_261:g.69272C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1889C>G	ENSP00000502725.1:p.Pro630Arg
ENST00000392302.7:c.1889C>G	ENSP00000376120.3:p.Pro630Arg
ENST00000497019.7:c.*661C>G	ENSP00000436804.2:n.*661C>G
ENST00000524377.7:c.2069C>G MANE Select	ENSP00000431418.1:p.Pro690Arg
ENST00000531606.2:c.37C>G
ENST00000674537.1:c.1889C>G	ENSP00000502725.1:p.Pro630Arg
ENST00000358660.3:c.2060C>G	ENSP00000351486.3:p.Pro687Arg
ENST00000368196.7:c.2051C>G	ENSP00000357179.3:p.Pro684Arg
ENST00000392302.6:c.1961C>G	ENSP00000376120.2:p.Pro654Arg
ENST00000497019.6:c.*661C>G	ENSP00000436804.1:n.*661C>G
ENST00000524377.5:c.2069C>G	ENSP00000431418.1:p.Pro690Arg
ENST00000530298.5:n.2522C>G
ENST00000531606.1:n.21C>G
NM_001007792.1:c.1961C>G , LRG_261t1:c.1961C>G	NP_001007793.1:p.Pro654Arg
NM_001012331.1:c.2051C>G , LRG_261t2:c.2051C>G	NP_001012331.1:p.Pro684Arg
NM_002529.3:c.2069C>G , LRG_261t3:c.2069C>G	NP_002520.2:p.Pro690Arg
NM_001012331.2:c.2051C>G	NP_001012331.1:p.Pro684Arg
NM_002529.4:c.2069C>G MANE Select	NP_002520.2:p.Pro690Arg