Canonical Allele Identifier: CA421138449

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102919026
• MyVariant Identifiers: chr1:g.156846194A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876402A>C , CM000663.2:g.156876402A>C	GRCh38
NC_000001.10:g.156846194A>C , CM000663.1:g.156846194A>C	GRCh37
NC_000001.9:g.155112818A>C	NCBI36
NG_007493.1:g.65653A>C , LRG_261:g.65653A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1455A>C	ENSP00000502725.1:p.Ala485=
ENST00000392302.7:c.1455A>C	ENSP00000376120.3:p.Ala485=
ENST00000497019.7:c.*227A>C	ENSP00000436804.2:n.*227A>C
ENST00000524377.7:c.1635A>C MANE Select	ENSP00000431418.1:p.Ala545=
ENST00000674537.1:c.1455A>C	ENSP00000502725.1:p.Ala485=
ENST00000358660.3:c.1626A>C	ENSP00000351486.3:p.Ala542=
ENST00000368196.7:c.1617A>C	ENSP00000357179.3:p.Ala539=
ENST00000392302.6:c.1527A>C	ENSP00000376120.2:p.Ala509=
ENST00000497019.6:c.*227A>C	ENSP00000436804.1:n.*227A>C
ENST00000524377.5:c.1635A>C	ENSP00000431418.1:p.Ala545=
ENST00000530298.5:n.2088A>C
NM_001007792.1:c.1527A>C , LRG_261t1:c.1527A>C	NP_001007793.1:p.Ala509=
NM_001012331.1:c.1617A>C , LRG_261t2:c.1617A>C	NP_001012331.1:p.Ala539=
NM_002529.3:c.1635A>C , LRG_261t3:c.1635A>C	NP_002520.2:p.Ala545=
NM_001012331.2:c.1617A>C	NP_001012331.1:p.Ala539=
NM_002529.4:c.1635A>C MANE Select	NP_002520.2:p.Ala545=