Canonical Allele Identifier: CA342937966

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917426
• MyVariant Identifiers: chr1:g.156845924G>C (hg19) ; chr1:g.156876132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876132G>C , CM000663.2:g.156876132G>C	GRCh38
NC_000001.10:g.156845924G>C , CM000663.1:g.156845924G>C	GRCh37
NC_000001.9:g.155112548G>C	NCBI36
NG_007493.1:g.65383G>C , LRG_261:g.65383G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1374G>C	ENSP00000502725.1:p.Glu458Asp
ENST00000392302.7:c.1374G>C	ENSP00000376120.3:p.Glu458Asp
ENST00000497019.7:c.*146G>C	ENSP00000436804.2:n.*146G>C
ENST00000524377.7:c.1554G>C MANE Select	ENSP00000431418.1:p.Glu518Asp
ENST00000674537.1:c.1374G>C	ENSP00000502725.1:p.Glu458Asp
ENST00000358660.3:c.1545G>C	ENSP00000351486.3:p.Glu515Asp
ENST00000368196.7:c.1536G>C	ENSP00000357179.3:p.Glu512Asp
ENST00000392302.6:c.1446G>C	ENSP00000376120.2:p.Glu482Asp
ENST00000497019.6:c.*146G>C	ENSP00000436804.1:n.*146G>C
ENST00000524377.5:c.1554G>C	ENSP00000431418.1:p.Glu518Asp
ENST00000530298.5:n.2007G>C
ENST00000534682.1:n.777G>C
NM_001007792.1:c.1446G>C , LRG_261t1:c.1446G>C	NP_001007793.1:p.Glu482Asp
NM_001012331.1:c.1536G>C , LRG_261t2:c.1536G>C	NP_001012331.1:p.Glu512Asp
NM_002529.3:c.1554G>C , LRG_261t3:c.1554G>C	NP_002520.2:p.Glu518Asp
NM_001012331.2:c.1536G>C	NP_001012331.1:p.Glu512Asp
NM_002529.4:c.1554G>C MANE Select	NP_002520.2:p.Glu518Asp