Canonical Allele Identifier: CA421138499

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 2785115
• ClinVar RCV Id: RCV003624644
• dbSNP Id: rs771010259
• gnomAD v4: 1-156876414-G-C
• MyVariant Identifiers: chr1:g.156846206G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876414G>C , CM000663.2:g.156876414G>C	GRCh38
NC_000001.10:g.156846206G>C , CM000663.1:g.156846206G>C	GRCh37
NC_000001.9:g.155112830G>C	NCBI36
NG_007493.1:g.65665G>C , LRG_261:g.65665G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1467G>C	ENSP00000502725.1:p.Ala489=
ENST00000392302.7:c.1467G>C	ENSP00000376120.3:p.Ala489=
ENST00000497019.7:c.*239G>C	ENSP00000436804.2:n.*239G>C
ENST00000524377.7:c.1647G>C MANE Select	ENSP00000431418.1:p.Ala549=
ENST00000674537.1:c.1467G>C	ENSP00000502725.1:p.Ala489=
ENST00000358660.3:c.1638G>C	ENSP00000351486.3:p.Ala546=
ENST00000368196.7:c.1629G>C	ENSP00000357179.3:p.Ala543=
ENST00000392302.6:c.1539G>C	ENSP00000376120.2:p.Ala513=
ENST00000497019.6:c.*239G>C	ENSP00000436804.1:n.*239G>C
ENST00000524377.5:c.1647G>C	ENSP00000431418.1:p.Ala549=
ENST00000530298.5:n.2100G>C
NM_001007792.1:c.1539G>C , LRG_261t1:c.1539G>C	NP_001007793.1:p.Ala513=
NM_001012331.1:c.1629G>C , LRG_261t2:c.1629G>C	NP_001012331.1:p.Ala543=
NM_002529.3:c.1647G>C , LRG_261t3:c.1647G>C	NP_002520.2:p.Ala549=
NM_001012331.2:c.1629G>C	NP_001012331.1:p.Ala543=
NM_002529.4:c.1647G>C MANE Select	NP_002520.2:p.Ala549=