Canonical Allele Identifier: CA421138085

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 2045828
• ClinVar RCV Id: RCV002900624
• MyVariant Identifiers: chr1:g.156845936G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876144G>A , CM000663.2:g.156876144G>A	GRCh38
NC_000001.10:g.156845936G>A , CM000663.1:g.156845936G>A	GRCh37
NC_000001.9:g.155112560G>A	NCBI36
NG_007493.1:g.65395G>A , LRG_261:g.65395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1386G>A	ENSP00000502725.1:p.Gly462=
ENST00000392302.7:c.1386G>A	ENSP00000376120.3:p.Gly462=
ENST00000497019.7:c.*158G>A	ENSP00000436804.2:n.*158G>A
ENST00000524377.7:c.1566G>A MANE Select	ENSP00000431418.1:p.Gly522=
ENST00000674537.1:c.1386G>A	ENSP00000502725.1:p.Gly462=
ENST00000358660.3:c.1557G>A	ENSP00000351486.3:p.Gly519=
ENST00000368196.7:c.1548G>A	ENSP00000357179.3:p.Gly516=
ENST00000392302.6:c.1458G>A	ENSP00000376120.2:p.Gly486=
ENST00000497019.6:c.*158G>A	ENSP00000436804.1:n.*158G>A
ENST00000524377.5:c.1566G>A	ENSP00000431418.1:p.Gly522=
ENST00000530298.5:n.2019G>A
ENST00000534682.1:n.789G>A
NM_001007792.1:c.1458G>A , LRG_261t1:c.1458G>A	NP_001007793.1:p.Gly486=
NM_001012331.1:c.1548G>A , LRG_261t2:c.1548G>A	NP_001012331.1:p.Gly516=
NM_002529.3:c.1566G>A , LRG_261t3:c.1566G>A	NP_002520.2:p.Gly522=
NM_001012331.2:c.1548G>A	NP_001012331.1:p.Gly516=
NM_002529.4:c.1566G>A MANE Select	NP_002520.2:p.Gly522=