Canonical Allele Identifier: CA342939396

Gene: NTRK1

Linked Data

• dbSNP Id: rs41470746
• COSMIC: COSM5609666 ; COSM5609667
• MyVariant Identifiers: chr1:g.156848922G>A (hg19) ; chr1:g.156879130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879130G>A , CM000663.2:g.156879130G>A	GRCh38
NC_000001.10:g.156848922G>A , CM000663.1:g.156848922G>A	GRCh37
NC_000001.9:g.155115546G>A	NCBI36
NG_007493.1:g.68381G>A , LRG_261:g.68381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1634G>A	ENSP00000502725.1:p.Gly545Glu
ENST00000392302.7:c.1634G>A	ENSP00000376120.3:p.Gly545Glu
ENST00000497019.7:c.*406G>A	ENSP00000436804.2:n.*406G>A
ENST00000524377.7:c.1814G>A MANE Select	ENSP00000431418.1:p.Gly605Glu
ENST00000674537.1:c.1634G>A	ENSP00000502725.1:p.Gly545Glu
ENST00000358660.3:c.1805G>A	ENSP00000351486.3:p.Gly602Glu
ENST00000368196.7:c.1796G>A	ENSP00000357179.3:p.Gly599Glu
ENST00000392302.6:c.1706G>A	ENSP00000376120.2:p.Gly569Glu
ENST00000497019.6:c.*406G>A	ENSP00000436804.1:n.*406G>A
ENST00000524377.5:c.1814G>A	ENSP00000431418.1:p.Gly605Glu
ENST00000530298.5:n.2267G>A
NM_001007792.1:c.1706G>A , LRG_261t1:c.1706G>A	NP_001007793.1:p.Gly569Glu
NM_001012331.1:c.1796G>A , LRG_261t2:c.1796G>A	NP_001012331.1:p.Gly599Glu
NM_002529.3:c.1814G>A , LRG_261t3:c.1814G>A	NP_002520.2:p.Gly605Glu
NM_001012331.2:c.1796G>A	NP_001012331.1:p.Gly599Glu
NM_002529.4:c.1814G>A MANE Select	NP_002520.2:p.Gly605Glu