Canonical Allele Identifier: CA421140445

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156849817T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880025T>A , CM000663.2:g.156880025T>A	GRCh38
NC_000001.10:g.156849817T>A , CM000663.1:g.156849817T>A	GRCh37
NC_000001.9:g.155116441T>A	NCBI36
NG_007493.1:g.69276T>A , LRG_261:g.69276T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1893T>A	ENSP00000502725.1:p.Ile631=
ENST00000392302.7:c.1893T>A	ENSP00000376120.3:p.Ile631=
ENST00000497019.7:c.*665T>A	ENSP00000436804.2:n.*665T>A
ENST00000524377.7:c.2073T>A MANE Select	ENSP00000431418.1:p.Ile691=
ENST00000531606.2:c.41T>A
ENST00000674537.1:c.1893T>A	ENSP00000502725.1:p.Ile631=
ENST00000358660.3:c.2064T>A	ENSP00000351486.3:p.Ile688=
ENST00000368196.7:c.2055T>A	ENSP00000357179.3:p.Ile685=
ENST00000392302.6:c.1965T>A	ENSP00000376120.2:p.Ile655=
ENST00000497019.6:c.*665T>A	ENSP00000436804.1:n.*665T>A
ENST00000524377.5:c.2073T>A	ENSP00000431418.1:p.Ile691=
ENST00000530298.5:n.2526T>A
ENST00000531606.1:n.25T>A
NM_001007792.1:c.1965T>A , LRG_261t1:c.1965T>A	NP_001007793.1:p.Ile655=
NM_001012331.1:c.2055T>A , LRG_261t2:c.2055T>A	NP_001012331.1:p.Ile685=
NM_002529.3:c.2073T>A , LRG_261t3:c.2073T>A	NP_002520.2:p.Ile691=
NM_001012331.2:c.2055T>A	NP_001012331.1:p.Ile685=
NM_002529.4:c.2073T>A MANE Select	NP_002520.2:p.Ile691=