Canonical Allele Identifier: CA342937200

Gene: NTRK1

Linked Data

• dbSNP Id: rs1647849526
• MyVariant Identifiers: chr1:g.156845317G>C (hg19) ; chr1:g.156875525G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875525G>C , CM000663.2:g.156875525G>C	GRCh38
NC_000001.10:g.156845317G>C , CM000663.1:g.156845317G>C	GRCh37
NC_000001.9:g.155111941G>C	NCBI36
NG_007493.1:g.64776G>C , LRG_261:g.64776G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1180G>C	ENSP00000502725.1:p.Ala394Pro
ENST00000392302.7:c.1180G>C	ENSP00000376120.3:p.Ala394Pro
ENST00000497019.7:c.1047G>C	ENSP00000436804.2:p.Arg349=
ENST00000524377.7:c.1360G>C MANE Select	ENSP00000431418.1:p.Ala454Pro
ENST00000674537.1:c.1180G>C	ENSP00000502725.1:p.Ala394Pro
ENST00000358660.3:c.1342G>C	ENSP00000351486.3:p.Ala448Pro
ENST00000368196.7:c.1342G>C	ENSP00000357179.3:p.Ala448Pro
ENST00000392302.6:c.1252G>C	ENSP00000376120.2:p.Ala418Pro
ENST00000497019.6:c.1119G>C	ENSP00000436804.1:p.Arg373=
ENST00000524377.5:c.1360G>C	ENSP00000431418.1:p.Ala454Pro
ENST00000530298.5:n.1400G>C
ENST00000534682.1:n.583G>C
NM_001007792.1:c.1252G>C , LRG_261t1:c.1252G>C	NP_001007793.1:p.Ala418Pro
NM_001012331.1:c.1342G>C , LRG_261t2:c.1342G>C	NP_001012331.1:p.Ala448Pro
NM_002529.3:c.1360G>C , LRG_261t3:c.1360G>C	NP_002520.2:p.Ala454Pro
NM_001012331.2:c.1342G>C	NP_001012331.1:p.Ala448Pro
NM_002529.4:c.1360G>C MANE Select	NP_002520.2:p.Ala454Pro