Canonical Allele Identifier: CA421138105

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917553
• COSMIC: COSM4468996 ; COSM4468997
• MyVariant Identifiers: chr1:g.156845945C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876153C>T , CM000663.2:g.156876153C>T	GRCh38
NC_000001.10:g.156845945C>T , CM000663.1:g.156845945C>T	GRCh37
NC_000001.9:g.155112569C>T	NCBI36
NG_007493.1:g.65404C>T , LRG_261:g.65404C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1395C>T	ENSP00000502725.1:p.Phe465=
ENST00000392302.7:c.1395C>T	ENSP00000376120.3:p.Phe465=
ENST00000497019.7:c.*167C>T	ENSP00000436804.2:n.*167C>T
ENST00000524377.7:c.1575C>T MANE Select	ENSP00000431418.1:p.Phe525=
ENST00000674537.1:c.1395C>T	ENSP00000502725.1:p.Phe465=
ENST00000358660.3:c.1566C>T	ENSP00000351486.3:p.Phe522=
ENST00000368196.7:c.1557C>T	ENSP00000357179.3:p.Phe519=
ENST00000392302.6:c.1467C>T	ENSP00000376120.2:p.Phe489=
ENST00000497019.6:c.*167C>T	ENSP00000436804.1:n.*167C>T
ENST00000524377.5:c.1575C>T	ENSP00000431418.1:p.Phe525=
ENST00000530298.5:n.2028C>T
ENST00000534682.1:n.798C>T
NM_001007792.1:c.1467C>T , LRG_261t1:c.1467C>T	NP_001007793.1:p.Phe489=
NM_001012331.1:c.1557C>T , LRG_261t2:c.1557C>T	NP_001012331.1:p.Phe519=
NM_002529.3:c.1575C>T , LRG_261t3:c.1575C>T	NP_002520.2:p.Phe525=
NM_001012331.2:c.1557C>T	NP_001012331.1:p.Phe519=
NM_002529.4:c.1575C>T MANE Select	NP_002520.2:p.Phe525=