Canonical Allele Identifier: CA342939551

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102924330
• gnomAD v4: 1-156879177-C-T
• MyVariant Identifiers: chr1:g.156848969C>T (hg19) ; chr1:g.156879177C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879177C>T , CM000663.2:g.156879177C>T	GRCh38
NC_000001.10:g.156848969C>T , CM000663.1:g.156848969C>T	GRCh37
NC_000001.9:g.155115593C>T	NCBI36
NG_007493.1:g.68428C>T , LRG_261:g.68428C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1681C>T	ENSP00000502725.1:p.Pro561Ser
ENST00000392302.7:c.1681C>T	ENSP00000376120.3:p.Pro561Ser
ENST00000497019.7:c.*453C>T	ENSP00000436804.2:n.*453C>T
ENST00000524377.7:c.1861C>T MANE Select	ENSP00000431418.1:p.Pro621Ser
ENST00000674537.1:c.1681C>T	ENSP00000502725.1:p.Pro561Ser
ENST00000358660.3:c.1852C>T	ENSP00000351486.3:p.Pro618Ser
ENST00000368196.7:c.1843C>T	ENSP00000357179.3:p.Pro615Ser
ENST00000392302.6:c.1753C>T	ENSP00000376120.2:p.Pro585Ser
ENST00000497019.6:c.*453C>T	ENSP00000436804.1:n.*453C>T
ENST00000524377.5:c.1861C>T	ENSP00000431418.1:p.Pro621Ser
ENST00000530298.5:n.2314C>T
NM_001007792.1:c.1753C>T , LRG_261t1:c.1753C>T	NP_001007793.1:p.Pro585Ser
NM_001012331.1:c.1843C>T , LRG_261t2:c.1843C>T	NP_001012331.1:p.Pro615Ser
NM_002529.3:c.1861C>T , LRG_261t3:c.1861C>T	NP_002520.2:p.Pro621Ser
NM_001012331.2:c.1843C>T	NP_001012331.1:p.Pro615Ser
NM_002529.4:c.1861C>T MANE Select	NP_002520.2:p.Pro621Ser