Canonical Allele Identifier: CA421140678

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102931414
• MyVariant Identifiers: chr1:g.156851389A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881597A>G , CM000663.2:g.156881597A>G	GRCh38
NC_000001.10:g.156851389A>G , CM000663.1:g.156851389A>G	GRCh37
NC_000001.9:g.155118013A>G	NCBI36
NG_007493.1:g.70848A>G , LRG_261:g.70848A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2166A>G	ENSP00000502725.1:p.Gln722=
ENST00000392302.7:c.2166A>G	ENSP00000376120.3:p.Gln722=
ENST00000497019.7:c.*938A>G	ENSP00000436804.2:n.*938A>G
ENST00000524377.7:c.2346A>G MANE Select	ENSP00000431418.1:p.Gln782=
ENST00000531606.2:c.405A>G
ENST00000674537.1:c.2166A>G	ENSP00000502725.1:p.Gln722=
ENST00000358660.3:c.2337A>G	ENSP00000351486.3:p.Gln779=
ENST00000368196.7:c.2328A>G	ENSP00000357179.3:p.Gln776=
ENST00000392302.6:c.2238A>G	ENSP00000376120.2:p.Gln746=
ENST00000497019.6:c.*938A>G	ENSP00000436804.1:n.*938A>G
ENST00000524377.5:c.2346A>G	ENSP00000431418.1:p.Gln782=
ENST00000530298.5:n.2799A>G
ENST00000531606.1:n.389A>G
NM_001007792.1:c.2238A>G , LRG_261t1:c.2238A>G	NP_001007793.1:p.Gln746=
NM_001012331.1:c.2328A>G , LRG_261t2:c.2328A>G	NP_001012331.1:p.Gln776=
NM_002529.3:c.2346A>G , LRG_261t3:c.2346A>G	NP_002520.2:p.Gln782=
NM_001012331.2:c.2328A>G	NP_001012331.1:p.Gln776=
NM_002529.4:c.2346A>G MANE Select	NP_002520.2:p.Gln782=