Canonical Allele Identifier: CA342928993

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156860965-G-T
• MyVariant Identifiers: chr1:g.156830757G>T (hg19) ; chr1:g.156860965G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860965G>T , CM000663.2:g.156860965G>T	GRCh38
NC_000001.10:g.156830757G>T , CM000663.1:g.156830757G>T	GRCh37
NC_000001.9:g.155097381G>T	NCBI36
NG_007493.1:g.50216G>T , LRG_261:g.50216G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3389G>T	ENSP00000502725.1:n.51-3389G>T
ENST00000392302.7:c.51-3389G>T	ENSP00000376120.3:n.51-3389G>T
ENST00000497019.7:c.51-3389G>T	ENSP00000436804.2:n.51-3389G>T
ENST00000524377.7:c.31G>T MANE Select	ENSP00000431418.1:p.Gly11Cys
ENST00000674537.1:c.51-3389G>T	ENSP00000502725.1:n.51-3389G>T
ENST00000675461.1:c.31G>T	ENSP00000501668.1:p.Gly11Cys
ENST00000358660.3:c.31G>T	ENSP00000351486.3:p.Gly11Cys
ENST00000368196.7:c.31G>T	ENSP00000357179.3:p.Gly11Cys
ENST00000392302.6:c.123-3389G>T	ENSP00000376120.2:n.123-3389G>T
ENST00000489021.6:n.313-12668G>T
ENST00000497019.6:c.123-3389G>T	ENSP00000436804.1:n.123-3389G>T
ENST00000524377.5:c.31G>T	ENSP00000431418.1:p.Gly11Cys
ENST00000530298.5:n.271-3389G>T
ENST00000533630.1:n.53G>T
NM_001007792.1:c.123-3389G>T , LRG_261t1:c.123-3389G>T	NP_001007793.1:n.123-3389G>T
NM_001012331.1:c.31G>T , LRG_261t2:c.31G>T	NP_001012331.1:p.Gly11Cys
NM_002529.3:c.31G>T , LRG_261t3:c.31G>T	NP_002520.2:p.Gly11Cys
NM_001012331.2:c.31G>T	NP_001012331.1:p.Gly11Cys
NM_002529.4:c.31G>T MANE Select	NP_002520.2:p.Gly11Cys