Canonical Allele Identifier: CA31118740

Gene: NTRK1

Linked Data

• dbSNP Id: rs562829243
• MyVariant Identifiers: chr1:g.156846222C>T (hg19) ; chr1:g.156876430C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876430C>T , CM000663.2:g.156876430C>T	GRCh38
NC_000001.10:g.156846222C>T , CM000663.1:g.156846222C>T	GRCh37
NC_000001.9:g.155112846C>T	NCBI36
NG_007493.1:g.65681C>T , LRG_261:g.65681C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1483C>T	ENSP00000502725.1:p.Gln495Ter
ENST00000392302.7:c.1483C>T	ENSP00000376120.3:p.Gln495Ter
ENST00000497019.7:c.*255C>T	ENSP00000436804.2:n.*255C>T
ENST00000524377.7:c.1663C>T MANE Select	ENSP00000431418.1:p.Gln555Ter
ENST00000674537.1:c.1483C>T	ENSP00000502725.1:p.Gln495Ter
ENST00000358660.3:c.1654C>T	ENSP00000351486.3:p.Gln552Ter
ENST00000368196.7:c.1645C>T	ENSP00000357179.3:p.Gln549Ter
ENST00000392302.6:c.1555C>T	ENSP00000376120.2:p.Gln519Ter
ENST00000497019.6:c.*255C>T	ENSP00000436804.1:n.*255C>T
ENST00000524377.5:c.1663C>T	ENSP00000431418.1:p.Gln555Ter
ENST00000530298.5:n.2116C>T
NM_001007792.1:c.1555C>T , LRG_261t1:c.1555C>T	NP_001007793.1:p.Gln519Ter
NM_001012331.1:c.1645C>T , LRG_261t2:c.1645C>T	NP_001012331.1:p.Gln549Ter
NM_002529.3:c.1663C>T , LRG_261t3:c.1663C>T	NP_002520.2:p.Gln555Ter
NM_001012331.2:c.1645C>T	NP_001012331.1:p.Gln549Ter
NM_002529.4:c.1663C>T MANE Select	NP_002520.2:p.Gln555Ter