Canonical Allele Identifier: CA342938427

Gene: NTRK1

Linked Data

• dbSNP Id: rs1647914323
• MyVariant Identifiers: chr1:g.156846211A>T (hg19) ; chr1:g.156876419A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876419A>T , CM000663.2:g.156876419A>T	GRCh38
NC_000001.10:g.156846211A>T , CM000663.1:g.156846211A>T	GRCh37
NC_000001.9:g.155112835A>T	NCBI36
NG_007493.1:g.65670A>T , LRG_261:g.65670A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1472A>T	ENSP00000502725.1:p.Glu491Val
ENST00000392302.7:c.1472A>T	ENSP00000376120.3:p.Glu491Val
ENST00000497019.7:c.*244A>T	ENSP00000436804.2:n.*244A>T
ENST00000524377.7:c.1652A>T MANE Select	ENSP00000431418.1:p.Glu551Val
ENST00000674537.1:c.1472A>T	ENSP00000502725.1:p.Glu491Val
ENST00000358660.3:c.1643A>T	ENSP00000351486.3:p.Glu548Val
ENST00000368196.7:c.1634A>T	ENSP00000357179.3:p.Glu545Val
ENST00000392302.6:c.1544A>T	ENSP00000376120.2:p.Glu515Val
ENST00000497019.6:c.*244A>T	ENSP00000436804.1:n.*244A>T
ENST00000524377.5:c.1652A>T	ENSP00000431418.1:p.Glu551Val
ENST00000530298.5:n.2105A>T
NM_001007792.1:c.1544A>T , LRG_261t1:c.1544A>T	NP_001007793.1:p.Glu515Val
NM_001012331.1:c.1634A>T , LRG_261t2:c.1634A>T	NP_001012331.1:p.Glu545Val
NM_002529.3:c.1652A>T , LRG_261t3:c.1652A>T	NP_002520.2:p.Glu551Val
NM_001012331.2:c.1634A>T	NP_001012331.1:p.Glu545Val
NM_002529.4:c.1652A>T MANE Select	NP_002520.2:p.Glu551Val