Canonical Allele Identifier: CA342940307

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880036C>A , CM000663.2:g.156880036C>A	GRCh38
NC_000001.10:g.156849828C>A , CM000663.1:g.156849828C>A	GRCh37
NC_000001.9:g.155116452C>A	NCBI36
NG_007493.1:g.69287C>A , LRG_261:g.69287C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1904C>A	ENSP00000502725.1:p.Pro635Gln
ENST00000392302.7:c.1904C>A	ENSP00000376120.3:p.Pro635Gln
ENST00000497019.7:c.*676C>A	ENSP00000436804.2:n.*676C>A
ENST00000524377.7:c.2084C>A MANE Select	ENSP00000431418.1:p.Pro695Gln
ENST00000531606.2:c.52C>A
ENST00000674537.1:c.1904C>A	ENSP00000502725.1:p.Pro635Gln
ENST00000358660.3:c.2075C>A	ENSP00000351486.3:p.Pro692Gln
ENST00000368196.7:c.2066C>A	ENSP00000357179.3:p.Pro689Gln
ENST00000392302.6:c.1976C>A	ENSP00000376120.2:p.Pro659Gln
ENST00000497019.6:c.*676C>A	ENSP00000436804.1:n.*676C>A
ENST00000524377.5:c.2084C>A	ENSP00000431418.1:p.Pro695Gln
ENST00000530298.5:n.2537C>A
ENST00000531606.1:n.36C>A
NM_001007792.1:c.1976C>A , LRG_261t1:c.1976C>A	NP_001007793.1:p.Pro659Gln
NM_001012331.1:c.2066C>A , LRG_261t2:c.2066C>A	NP_001012331.1:p.Pro689Gln
NM_002529.3:c.2084C>A , LRG_261t3:c.2084C>A	NP_002520.2:p.Pro695Gln
NM_001012331.2:c.2066C>A	NP_001012331.1:p.Pro689Gln
NM_002529.4:c.2084C>A MANE Select	NP_002520.2:p.Pro695Gln