Canonical Allele Identifier: CA342940280

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156849821T>G (hg19) ; chr1:g.156880029T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880029T>G , CM000663.2:g.156880029T>G	GRCh38
NC_000001.10:g.156849821T>G , CM000663.1:g.156849821T>G	GRCh37
NC_000001.9:g.155116445T>G	NCBI36
NG_007493.1:g.69280T>G , LRG_261:g.69280T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1897T>G	ENSP00000502725.1:p.Trp633Gly
ENST00000392302.7:c.1897T>G	ENSP00000376120.3:p.Trp633Gly
ENST00000497019.7:c.*669T>G	ENSP00000436804.2:n.*669T>G
ENST00000524377.7:c.2077T>G MANE Select	ENSP00000431418.1:p.Trp693Gly
ENST00000531606.2:c.45T>G
ENST00000674537.1:c.1897T>G	ENSP00000502725.1:p.Trp633Gly
ENST00000358660.3:c.2068T>G	ENSP00000351486.3:p.Trp690Gly
ENST00000368196.7:c.2059T>G	ENSP00000357179.3:p.Trp687Gly
ENST00000392302.6:c.1969T>G	ENSP00000376120.2:p.Trp657Gly
ENST00000497019.6:c.*669T>G	ENSP00000436804.1:n.*669T>G
ENST00000524377.5:c.2077T>G	ENSP00000431418.1:p.Trp693Gly
ENST00000530298.5:n.2530T>G
ENST00000531606.1:n.29T>G
NM_001007792.1:c.1969T>G , LRG_261t1:c.1969T>G	NP_001007793.1:p.Trp657Gly
NM_001012331.1:c.2059T>G , LRG_261t2:c.2059T>G	NP_001012331.1:p.Trp687Gly
NM_002529.3:c.2077T>G , LRG_261t3:c.2077T>G	NP_002520.2:p.Trp693Gly
NM_001012331.2:c.2059T>G	NP_001012331.1:p.Trp687Gly
NM_002529.4:c.2077T>G MANE Select	NP_002520.2:p.Trp693Gly