Canonical Allele Identifier: CA342940051

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879336G>C , CM000663.2:g.156879336G>C	GRCh38
NC_000001.10:g.156849128G>C , CM000663.1:g.156849128G>C	GRCh37
NC_000001.9:g.155115752G>C	NCBI36
NG_007493.1:g.68587G>C , LRG_261:g.68587G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1840G>C	ENSP00000502725.1:p.Asp614His
ENST00000392302.7:c.1840G>C	ENSP00000376120.3:p.Asp614His
ENST00000497019.7:c.*612G>C	ENSP00000436804.2:n.*612G>C
ENST00000524377.7:c.2020G>C MANE Select	ENSP00000431418.1:p.Asp674His
ENST00000674537.1:c.1840G>C	ENSP00000502725.1:p.Asp614His
ENST00000358660.3:c.2011G>C	ENSP00000351486.3:p.Asp671His
ENST00000368196.7:c.2002G>C	ENSP00000357179.3:p.Asp668His
ENST00000392302.6:c.1912G>C	ENSP00000376120.2:p.Asp638His
ENST00000497019.6:c.*612G>C	ENSP00000436804.1:n.*612G>C
ENST00000524377.5:c.2020G>C	ENSP00000431418.1:p.Asp674His
ENST00000530298.5:n.2473G>C
NM_001007792.1:c.1912G>C , LRG_261t1:c.1912G>C	NP_001007793.1:p.Asp638His
NM_001012331.1:c.2002G>C , LRG_261t2:c.2002G>C	NP_001012331.1:p.Asp668His
NM_002529.3:c.2020G>C , LRG_261t3:c.2020G>C	NP_002520.2:p.Asp674His
NM_001012331.2:c.2002G>C	NP_001012331.1:p.Asp668His
NM_002529.4:c.2020G>C MANE Select	NP_002520.2:p.Asp674His