Canonical Allele Identifier: CA342940273

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156880026-C-A
• MyVariant Identifiers: chr1:g.156849818C>A (hg19) ; chr1:g.156880026C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880026C>A , CM000663.2:g.156880026C>A	GRCh38
NC_000001.10:g.156849818C>A , CM000663.1:g.156849818C>A	GRCh37
NC_000001.9:g.155116442C>A	NCBI36
NG_007493.1:g.69277C>A , LRG_261:g.69277C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1894C>A	ENSP00000502725.1:p.Arg632Ser
ENST00000392302.7:c.1894C>A	ENSP00000376120.3:p.Arg632Ser
ENST00000497019.7:c.*666C>A	ENSP00000436804.2:n.*666C>A
ENST00000524377.7:c.2074C>A MANE Select	ENSP00000431418.1:p.Arg692Ser
ENST00000531606.2:c.42C>A
ENST00000674537.1:c.1894C>A	ENSP00000502725.1:p.Arg632Ser
ENST00000358660.3:c.2065C>A	ENSP00000351486.3:p.Arg689Ser
ENST00000368196.7:c.2056C>A	ENSP00000357179.3:p.Arg686Ser
ENST00000392302.6:c.1966C>A	ENSP00000376120.2:p.Arg656Ser
ENST00000497019.6:c.*666C>A	ENSP00000436804.1:n.*666C>A
ENST00000524377.5:c.2074C>A	ENSP00000431418.1:p.Arg692Ser
ENST00000530298.5:n.2527C>A
ENST00000531606.1:n.26C>A
NM_001007792.1:c.1966C>A , LRG_261t1:c.1966C>A	NP_001007793.1:p.Arg656Ser
NM_001012331.1:c.2056C>A , LRG_261t2:c.2056C>A	NP_001012331.1:p.Arg686Ser
NM_002529.3:c.2074C>A , LRG_261t3:c.2074C>A	NP_002520.2:p.Arg692Ser
NM_001012331.2:c.2056C>A	NP_001012331.1:p.Arg686Ser
NM_002529.4:c.2074C>A MANE Select	NP_002520.2:p.Arg692Ser