Canonical Allele Identifier: CA421137225

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156875620-G-T
• MyVariant Identifiers: chr1:g.156845412G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875620G>T , CM000663.2:g.156875620G>T	GRCh38
NC_000001.10:g.156845412G>T , CM000663.1:g.156845412G>T	GRCh37
NC_000001.9:g.155112036G>T	NCBI36
NG_007493.1:g.64871G>T , LRG_261:g.64871G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1275G>T	ENSP00000502725.1:p.Gly425=
ENST00000392302.7:c.1275G>T	ENSP00000376120.3:p.Gly425=
ENST00000497019.7:c.*47G>T	ENSP00000436804.2:n.*47G>T
ENST00000524377.7:c.1455G>T MANE Select	ENSP00000431418.1:p.Gly485=
ENST00000674537.1:c.1275G>T	ENSP00000502725.1:p.Gly425=
ENST00000358660.3:c.1437G>T	ENSP00000351486.3:p.Gly479=
ENST00000368196.7:c.1437G>T	ENSP00000357179.3:p.Gly479=
ENST00000392302.6:c.1347G>T	ENSP00000376120.2:p.Gly449=
ENST00000497019.6:c.*47G>T	ENSP00000436804.1:n.*47G>T
ENST00000524377.5:c.1455G>T	ENSP00000431418.1:p.Gly485=
ENST00000530298.5:n.1495G>T
ENST00000534682.1:n.678G>T
NM_001007792.1:c.1347G>T , LRG_261t1:c.1347G>T	NP_001007793.1:p.Gly449=
NM_001012331.1:c.1437G>T , LRG_261t2:c.1437G>T	NP_001012331.1:p.Gly479=
NM_002529.3:c.1455G>T , LRG_261t3:c.1455G>T	NP_002520.2:p.Gly485=
NM_001012331.2:c.1437G>T	NP_001012331.1:p.Gly479=
NM_002529.4:c.1455G>T MANE Select	NP_002520.2:p.Gly485=