Canonical Allele Identifier: CA342941713

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156851372G>T (hg19) ; chr1:g.156881580G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881580G>T , CM000663.2:g.156881580G>T	GRCh38
NC_000001.10:g.156851372G>T , CM000663.1:g.156851372G>T	GRCh37
NC_000001.9:g.155117996G>T	NCBI36
NG_007493.1:g.70831G>T , LRG_261:g.70831G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2149G>T	ENSP00000502725.1:p.Val717Leu
ENST00000392302.7:c.2149G>T	ENSP00000376120.3:p.Val717Leu
ENST00000497019.7:c.*921G>T	ENSP00000436804.2:n.*921G>T
ENST00000524377.7:c.2329G>T MANE Select	ENSP00000431418.1:p.Val777Leu
ENST00000531606.2:c.388G>T
ENST00000674537.1:c.2149G>T	ENSP00000502725.1:p.Val717Leu
ENST00000358660.3:c.2320G>T	ENSP00000351486.3:p.Val774Leu
ENST00000368196.7:c.2311G>T	ENSP00000357179.3:p.Val771Leu
ENST00000392302.6:c.2221G>T	ENSP00000376120.2:p.Val741Leu
ENST00000497019.6:c.*921G>T	ENSP00000436804.1:n.*921G>T
ENST00000524377.5:c.2329G>T	ENSP00000431418.1:p.Val777Leu
ENST00000530298.5:n.2782G>T
ENST00000531606.1:n.372G>T
NM_001007792.1:c.2221G>T , LRG_261t1:c.2221G>T	NP_001007793.1:p.Val741Leu
NM_001012331.1:c.2311G>T , LRG_261t2:c.2311G>T	NP_001012331.1:p.Val771Leu
NM_002529.3:c.2329G>T , LRG_261t3:c.2329G>T	NP_002520.2:p.Val777Leu
NM_001012331.2:c.2311G>T	NP_001012331.1:p.Val771Leu
NM_002529.4:c.2329G>T MANE Select	NP_002520.2:p.Val777Leu