Canonical Allele Identifier: CA342939514

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156848955A>C (hg19) ; chr1:g.156879163A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879163A>C , CM000663.2:g.156879163A>C	GRCh38
NC_000001.10:g.156848955A>C , CM000663.1:g.156848955A>C	GRCh37
NC_000001.9:g.155115579A>C	NCBI36
NG_007493.1:g.68414A>C , LRG_261:g.68414A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1667A>C	ENSP00000502725.1:p.Asp556Ala
ENST00000392302.7:c.1667A>C	ENSP00000376120.3:p.Asp556Ala
ENST00000497019.7:c.*439A>C	ENSP00000436804.2:n.*439A>C
ENST00000524377.7:c.1847A>C MANE Select	ENSP00000431418.1:p.Asp616Ala
ENST00000674537.1:c.1667A>C	ENSP00000502725.1:p.Asp556Ala
ENST00000358660.3:c.1838A>C	ENSP00000351486.3:p.Asp613Ala
ENST00000368196.7:c.1829A>C	ENSP00000357179.3:p.Asp610Ala
ENST00000392302.6:c.1739A>C	ENSP00000376120.2:p.Asp580Ala
ENST00000497019.6:c.*439A>C	ENSP00000436804.1:n.*439A>C
ENST00000524377.5:c.1847A>C	ENSP00000431418.1:p.Asp616Ala
ENST00000530298.5:n.2300A>C
NM_001007792.1:c.1739A>C , LRG_261t1:c.1739A>C	NP_001007793.1:p.Asp580Ala
NM_001012331.1:c.1829A>C , LRG_261t2:c.1829A>C	NP_001012331.1:p.Asp610Ala
NM_002529.3:c.1847A>C , LRG_261t3:c.1847A>C	NP_002520.2:p.Asp616Ala
NM_001012331.2:c.1829A>C	NP_001012331.1:p.Asp610Ala
NM_002529.4:c.1847A>C MANE Select	NP_002520.2:p.Asp616Ala