Canonical Allele Identifier: CA421271844

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156849064C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879272C>G , CM000663.2:g.156879272C>G	GRCh38
NC_000001.10:g.156849064C>G , CM000663.1:g.156849064C>G	GRCh37
NC_000001.9:g.155115688C>G	NCBI36
NG_007493.1:g.68523C>G , LRG_261:g.68523C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1776C>G	ENSP00000502725.1:p.Ala592=
ENST00000392302.7:c.1776C>G	ENSP00000376120.3:p.Ala592=
ENST00000497019.7:c.*548C>G	ENSP00000436804.2:n.*548C>G
ENST00000524377.7:c.1956C>G MANE Select	ENSP00000431418.1:p.Ala652=
ENST00000674537.1:c.1776C>G	ENSP00000502725.1:p.Ala592=
ENST00000358660.3:c.1947C>G	ENSP00000351486.3:p.Ala649=
ENST00000368196.7:c.1938C>G	ENSP00000357179.3:p.Ala646=
ENST00000392302.6:c.1848C>G	ENSP00000376120.2:p.Ala616=
ENST00000497019.6:c.*548C>G	ENSP00000436804.1:n.*548C>G
ENST00000524377.5:c.1956C>G	ENSP00000431418.1:p.Ala652=
ENST00000530298.5:n.2409C>G
NM_001007792.1:c.1848C>G , LRG_261t1:c.1848C>G	NP_001007793.1:p.Ala616=
NM_001012331.1:c.1938C>G , LRG_261t2:c.1938C>G	NP_001012331.1:p.Ala646=
NM_002529.3:c.1956C>G , LRG_261t3:c.1956C>G	NP_002520.2:p.Ala652=
NM_001012331.2:c.1938C>G	NP_001012331.1:p.Ala646=
NM_002529.4:c.1956C>G MANE Select	NP_002520.2:p.Ala652=