Canonical Allele Identifier: CA342941672

Gene: NTRK1

Linked Data

• dbSNP Id: rs757985119
• MyVariant Identifiers: chr1:g.156851358A>C (hg19) ; chr1:g.156881566A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881566A>C , CM000663.2:g.156881566A>C	GRCh38
NC_000001.10:g.156851358A>C , CM000663.1:g.156851358A>C	GRCh37
NC_000001.9:g.155117982A>C	NCBI36
NG_007493.1:g.70817A>C , LRG_261:g.70817A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2135A>C	ENSP00000502725.1:p.His712Pro
ENST00000392302.7:c.2135A>C	ENSP00000376120.3:p.His712Pro
ENST00000497019.7:c.*907A>C	ENSP00000436804.2:n.*907A>C
ENST00000524377.7:c.2315A>C MANE Select	ENSP00000431418.1:p.His772Pro
ENST00000531606.2:c.374A>C
ENST00000674537.1:c.2135A>C	ENSP00000502725.1:p.His712Pro
ENST00000358660.3:c.2306A>C	ENSP00000351486.3:p.His769Pro
ENST00000368196.7:c.2297A>C	ENSP00000357179.3:p.His766Pro
ENST00000392302.6:c.2207A>C	ENSP00000376120.2:p.His736Pro
ENST00000497019.6:c.*907A>C	ENSP00000436804.1:n.*907A>C
ENST00000524377.5:c.2315A>C	ENSP00000431418.1:p.His772Pro
ENST00000530298.5:n.2768A>C
ENST00000531606.1:n.358A>C
NM_001007792.1:c.2207A>C , LRG_261t1:c.2207A>C	NP_001007793.1:p.His736Pro
NM_001012331.1:c.2297A>C , LRG_261t2:c.2297A>C	NP_001012331.1:p.His766Pro
NM_002529.3:c.2315A>C , LRG_261t3:c.2315A>C	NP_002520.2:p.His772Pro
NM_001012331.2:c.2297A>C	NP_001012331.1:p.His766Pro
NM_002529.4:c.2315A>C MANE Select	NP_002520.2:p.His772Pro