Canonical Allele Identifier: CA342937499

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156845404G>T (hg19) ; chr1:g.156875612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875612G>T , CM000663.2:g.156875612G>T	GRCh38
NC_000001.10:g.156845404G>T , CM000663.1:g.156845404G>T	GRCh37
NC_000001.9:g.155112028G>T	NCBI36
NG_007493.1:g.64863G>T , LRG_261:g.64863G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1267G>T	ENSP00000502725.1:p.Gly423Cys
ENST00000392302.7:c.1267G>T	ENSP00000376120.3:p.Gly423Cys
ENST00000497019.7:c.*39G>T	ENSP00000436804.2:n.*39G>T
ENST00000524377.7:c.1447G>T MANE Select	ENSP00000431418.1:p.Gly483Cys
ENST00000674537.1:c.1267G>T	ENSP00000502725.1:p.Gly423Cys
ENST00000358660.3:c.1429G>T	ENSP00000351486.3:p.Gly477Cys
ENST00000368196.7:c.1429G>T	ENSP00000357179.3:p.Gly477Cys
ENST00000392302.6:c.1339G>T	ENSP00000376120.2:p.Gly447Cys
ENST00000497019.6:c.*39G>T	ENSP00000436804.1:n.*39G>T
ENST00000524377.5:c.1447G>T	ENSP00000431418.1:p.Gly483Cys
ENST00000530298.5:n.1487G>T
ENST00000534682.1:n.670G>T
NM_001007792.1:c.1339G>T , LRG_261t1:c.1339G>T	NP_001007793.1:p.Gly447Cys
NM_001012331.1:c.1429G>T , LRG_261t2:c.1429G>T	NP_001012331.1:p.Gly477Cys
NM_002529.3:c.1447G>T , LRG_261t3:c.1447G>T	NP_002520.2:p.Gly483Cys
NM_001012331.2:c.1429G>T	NP_001012331.1:p.Gly477Cys
NM_002529.4:c.1447G>T MANE Select	NP_002520.2:p.Gly483Cys