Canonical Allele Identifier: CA421271677

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 1927841
• ClinVar RCV Id: RCV002621900
• dbSNP Id: rs41377846
• MyVariant Identifiers: chr1:g.156848950G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879158G>A , CM000663.2:g.156879158G>A	GRCh38
NC_000001.10:g.156848950G>A , CM000663.1:g.156848950G>A	GRCh37
NC_000001.9:g.155115574G>A	NCBI36
NG_007493.1:g.68409G>A , LRG_261:g.68409G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1662G>A	ENSP00000502725.1:p.Gly554=
ENST00000392302.7:c.1662G>A	ENSP00000376120.3:p.Gly554=
ENST00000497019.7:c.*434G>A	ENSP00000436804.2:n.*434G>A
ENST00000524377.7:c.1842G>A MANE Select	ENSP00000431418.1:p.Gly614=
ENST00000674537.1:c.1662G>A	ENSP00000502725.1:p.Gly554=
ENST00000358660.3:c.1833G>A	ENSP00000351486.3:p.Gly611=
ENST00000368196.7:c.1824G>A	ENSP00000357179.3:p.Gly608=
ENST00000392302.6:c.1734G>A	ENSP00000376120.2:p.Gly578=
ENST00000497019.6:c.*434G>A	ENSP00000436804.1:n.*434G>A
ENST00000524377.5:c.1842G>A	ENSP00000431418.1:p.Gly614=
ENST00000530298.5:n.2295G>A
NM_001007792.1:c.1734G>A , LRG_261t1:c.1734G>A	NP_001007793.1:p.Gly578=
NM_001012331.1:c.1824G>A , LRG_261t2:c.1824G>A	NP_001012331.1:p.Gly608=
NM_002529.3:c.1842G>A , LRG_261t3:c.1842G>A	NP_002520.2:p.Gly614=
NM_001012331.2:c.1824G>A	NP_001012331.1:p.Gly608=
NM_002529.4:c.1842G>A MANE Select	NP_002520.2:p.Gly614=