Canonical Allele Identifier: CA1169426

Gene: NTRK1

Linked Data

• dbSNP Id: rs776609372
• ExAC: 1:156846203 G / A
• gnomAD v2: 1-156846203-G-A
• gnomAD v4: 1-156876411-G-A
• MyVariant Identifiers: chr1:g.156846203G>A (hg19) ; chr1:g.156876411G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876411G>A , CM000663.2:g.156876411G>A	GRCh38
NC_000001.10:g.156846203G>A , CM000663.1:g.156846203G>A	GRCh37
NC_000001.9:g.155112827G>A	NCBI36
NG_007493.1:g.65662G>A , LRG_261:g.65662G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1464G>A	ENSP00000502725.1:p.Glu488=
ENST00000392302.7:c.1464G>A	ENSP00000376120.3:p.Glu488=
ENST00000497019.7:c.*236G>A	ENSP00000436804.2:n.*236G>A
ENST00000524377.7:c.1644G>A MANE Select	ENSP00000431418.1:p.Glu548=
ENST00000674537.1:c.1464G>A	ENSP00000502725.1:p.Glu488=
ENST00000358660.3:c.1635G>A	ENSP00000351486.3:p.Glu545=
ENST00000368196.7:c.1626G>A	ENSP00000357179.3:p.Glu542=
ENST00000392302.6:c.1536G>A	ENSP00000376120.2:p.Glu512=
ENST00000497019.6:c.*236G>A	ENSP00000436804.1:n.*236G>A
ENST00000524377.5:c.1644G>A	ENSP00000431418.1:p.Glu548=
ENST00000530298.5:n.2097G>A
NM_001007792.1:c.1536G>A , LRG_261t1:c.1536G>A	NP_001007793.1:p.Glu512=
NM_001012331.1:c.1626G>A , LRG_261t2:c.1626G>A	NP_001012331.1:p.Glu542=
NM_002529.3:c.1644G>A , LRG_261t3:c.1644G>A	NP_002520.2:p.Glu548=
NM_001012331.2:c.1626G>A	NP_001012331.1:p.Glu542=
NM_002529.4:c.1644G>A MANE Select	NP_002520.2:p.Glu548=