Canonical Allele Identifier: CA342932566

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156834536G>C (hg19) ; chr1:g.156864744G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156864744G>C , CM000663.2:g.156864744G>C	GRCh38
NC_000001.10:g.156834536G>C , CM000663.1:g.156834536G>C	GRCh37
NC_000001.9:g.155101160G>C	NCBI36
NG_007493.1:g.53995G>C , LRG_261:g.53995G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.142G>C	ENSP00000502725.1:p.Gly48Arg
ENST00000392302.7:c.142G>C	ENSP00000376120.3:p.Gly48Arg
ENST00000497019.7:c.142G>C	ENSP00000436804.2:p.Gly48Arg
ENST00000524377.7:c.304G>C MANE Select	ENSP00000431418.1:p.Gly102Arg
ENST00000674537.1:c.142G>C	ENSP00000502725.1:p.Gly48Arg
ENST00000675461.1:c.304G>C	ENSP00000501668.1:p.Gly102Arg
ENST00000358660.3:c.304G>C	ENSP00000351486.3:p.Gly102Arg
ENST00000368196.7:c.304G>C	ENSP00000357179.3:p.Gly102Arg
ENST00000392302.6:c.214G>C	ENSP00000376120.2:p.Gly72Arg
ENST00000489021.6:n.313-8889G>C
ENST00000497019.6:c.214G>C	ENSP00000436804.1:p.Gly72Arg
ENST00000524377.5:c.304G>C	ENSP00000431418.1:p.Gly102Arg
ENST00000530298.5:n.362G>C
ENST00000533630.1:n.326G>C
NM_001007792.1:c.214G>C , LRG_261t1:c.214G>C	NP_001007793.1:p.Gly72Arg
NM_001012331.1:c.304G>C , LRG_261t2:c.304G>C	NP_001012331.1:p.Gly102Arg
NM_002529.3:c.304G>C , LRG_261t3:c.304G>C	NP_002520.2:p.Gly102Arg
NM_001012331.2:c.304G>C	NP_001012331.1:p.Gly102Arg
NM_002529.4:c.304G>C MANE Select	NP_002520.2:p.Gly102Arg