Canonical Allele Identifier: CA342940404

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880066C>G , CM000663.2:g.156880066C>G	GRCh38
NC_000001.10:g.156849858C>G , CM000663.1:g.156849858C>G	GRCh37
NC_000001.9:g.155116482C>G	NCBI36
NG_007493.1:g.69317C>G , LRG_261:g.69317C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.2114C>G MANE Select	NP_002520.2:p.Thr705Ser
ENST00000524377.7:c.2114C>G MANE Select	ENSP00000431418.1:p.Thr705Ser
NM_001007792.1:c.2006C>G , LRG_261t1:c.2006C>G	NP_001007793.1:p.Thr669Ser
NM_001012331.1:c.2096C>G , LRG_261t2:c.2096C>G	NP_001012331.1:p.Thr699Ser
NM_001012331.2:c.2096C>G	NP_001012331.1:p.Thr699Ser
NM_002529.3:c.2114C>G , LRG_261t3:c.2114C>G	NP_002520.2:p.Thr705Ser
ENST00000358660.3:c.2105C>G	ENSP00000351486.3:p.Thr702Ser
ENST00000368196.7:c.2096C>G	ENSP00000357179.3:p.Thr699Ser
ENST00000392302.6:c.2006C>G	ENSP00000376120.2:p.Thr669Ser
ENST00000392302.7:c.1934C>G	ENSP00000376120.3:p.Thr645Ser
ENST00000497019.6:c.*706C>G	ENSP00000436804.1:n.*706C>G
ENST00000497019.7:c.*706C>G	ENSP00000436804.2:n.*706C>G
ENST00000524377.5:c.2114C>G	ENSP00000431418.1:p.Thr705Ser
ENST00000530298.5:n.2567C>G
ENST00000531606.1:n.66C>G
ENST00000531606.2:c.82C>G
ENST00000674537.1:c.1934C>G	ENSP00000502725.1:p.Thr645Ser
ENST00000674537.2:c.1934C>G	ENSP00000502725.1:p.Thr645Ser