Canonical Allele Identifier: CA342937817

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156845884T>G (hg19) ; chr1:g.156876092T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876092T>G , CM000663.2:g.156876092T>G	GRCh38
NC_000001.10:g.156845884T>G , CM000663.1:g.156845884T>G	GRCh37
NC_000001.9:g.155112508T>G	NCBI36
NG_007493.1:g.65343T>G , LRG_261:g.65343T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1334T>G	ENSP00000502725.1:p.Ile445Ser
ENST00000392302.7:c.1334T>G	ENSP00000376120.3:p.Ile445Ser
ENST00000497019.7:c.*106T>G	ENSP00000436804.2:n.*106T>G
ENST00000524377.7:c.1514T>G MANE Select	ENSP00000431418.1:p.Ile505Ser
ENST00000674537.1:c.1334T>G	ENSP00000502725.1:p.Ile445Ser
ENST00000358660.3:c.1505T>G	ENSP00000351486.3:p.Ile502Ser
ENST00000368196.7:c.1496T>G	ENSP00000357179.3:p.Ile499Ser
ENST00000392302.6:c.1406T>G	ENSP00000376120.2:p.Ile469Ser
ENST00000497019.6:c.*106T>G	ENSP00000436804.1:n.*106T>G
ENST00000524377.5:c.1514T>G	ENSP00000431418.1:p.Ile505Ser
ENST00000530298.5:n.1967T>G
ENST00000534682.1:n.737T>G
NM_001007792.1:c.1406T>G , LRG_261t1:c.1406T>G	NP_001007793.1:p.Ile469Ser
NM_001012331.1:c.1496T>G , LRG_261t2:c.1496T>G	NP_001012331.1:p.Ile499Ser
NM_002529.3:c.1514T>G , LRG_261t3:c.1514T>G	NP_002520.2:p.Ile505Ser
NM_001012331.2:c.1496T>G	NP_001012331.1:p.Ile499Ser
NM_002529.4:c.1514T>G MANE Select	NP_002520.2:p.Ile505Ser