Canonical Allele Identifier: CA342941605

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156881539-G-A
• MyVariant Identifiers: chr1:g.156851331G>A (hg19) ; chr1:g.156881539G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881539G>A , CM000663.2:g.156881539G>A	GRCh38
NC_000001.10:g.156851331G>A , CM000663.1:g.156851331G>A	GRCh37
NC_000001.9:g.155117955G>A	NCBI36
NG_007493.1:g.70790G>A , LRG_261:g.70790G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2108G>A	ENSP00000502725.1:p.Cys703Tyr
ENST00000392302.7:c.2108G>A	ENSP00000376120.3:p.Cys703Tyr
ENST00000497019.7:c.*880G>A	ENSP00000436804.2:n.*880G>A
ENST00000524377.7:c.2288G>A MANE Select	ENSP00000431418.1:p.Cys763Tyr
ENST00000531606.2:c.347G>A
ENST00000674537.1:c.2108G>A	ENSP00000502725.1:p.Cys703Tyr
ENST00000358660.3:c.2279G>A	ENSP00000351486.3:p.Cys760Tyr
ENST00000368196.7:c.2270G>A	ENSP00000357179.3:p.Cys757Tyr
ENST00000392302.6:c.2180G>A	ENSP00000376120.2:p.Cys727Tyr
ENST00000497019.6:c.*880G>A	ENSP00000436804.1:n.*880G>A
ENST00000524377.5:c.2288G>A	ENSP00000431418.1:p.Cys763Tyr
ENST00000530298.5:n.2741G>A
ENST00000531606.1:n.331G>A
NM_001007792.1:c.2180G>A , LRG_261t1:c.2180G>A	NP_001007793.1:p.Cys727Tyr
NM_001012331.1:c.2270G>A , LRG_261t2:c.2270G>A	NP_001012331.1:p.Cys757Tyr
NM_002529.3:c.2288G>A , LRG_261t3:c.2288G>A	NP_002520.2:p.Cys763Tyr
NM_001012331.2:c.2270G>A	NP_001012331.1:p.Cys757Tyr
NM_002529.4:c.2288G>A MANE Select	NP_002520.2:p.Cys763Tyr