Canonical Allele Identifier: CA342938192

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917772
• MyVariant Identifiers: chr1:g.156845980A>G (hg19) ; chr1:g.156876188A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876188A>G , CM000663.2:g.156876188A>G	GRCh38
NC_000001.10:g.156845980A>G , CM000663.1:g.156845980A>G	GRCh37
NC_000001.9:g.155112604A>G	NCBI36
NG_007493.1:g.65439A>G , LRG_261:g.65439A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1430A>G	ENSP00000502725.1:p.Asp477Gly
ENST00000392302.7:c.1430A>G	ENSP00000376120.3:p.Asp477Gly
ENST00000497019.7:c.*202A>G	ENSP00000436804.2:n.*202A>G
ENST00000524377.7:c.1610A>G MANE Select	ENSP00000431418.1:p.Asp537Gly
ENST00000674537.1:c.1430A>G	ENSP00000502725.1:p.Asp477Gly
ENST00000358660.3:c.1601A>G	ENSP00000351486.3:p.Asp534Gly
ENST00000368196.7:c.1592A>G	ENSP00000357179.3:p.Asp531Gly
ENST00000392302.6:c.1502A>G	ENSP00000376120.2:p.Asp501Gly
ENST00000497019.6:c.*202A>G	ENSP00000436804.1:n.*202A>G
ENST00000524377.5:c.1610A>G	ENSP00000431418.1:p.Asp537Gly
ENST00000530298.5:n.2063A>G
ENST00000534682.1:n.833A>G
NM_001007792.1:c.1502A>G , LRG_261t1:c.1502A>G	NP_001007793.1:p.Asp501Gly
NM_001012331.1:c.1592A>G , LRG_261t2:c.1592A>G	NP_001012331.1:p.Asp531Gly
NM_002529.3:c.1610A>G , LRG_261t3:c.1610A>G	NP_002520.2:p.Asp537Gly
NM_001012331.2:c.1592A>G	NP_001012331.1:p.Asp531Gly
NM_002529.4:c.1610A>G MANE Select	NP_002520.2:p.Asp537Gly