Canonical Allele Identifier: CA342941466

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102930735
• MyVariant Identifiers: chr1:g.156851288C>T (hg19) ; chr1:g.156881496C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881496C>T , CM000663.2:g.156881496C>T	GRCh38
NC_000001.10:g.156851288C>T , CM000663.1:g.156851288C>T	GRCh37
NC_000001.9:g.155117912C>T	NCBI36
NG_007493.1:g.70747C>T , LRG_261:g.70747C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.2065C>T	ENSP00000502725.1:p.Pro689Ser
ENST00000392302.7:c.2065C>T	ENSP00000376120.3:p.Pro689Ser
ENST00000497019.7:c.*837C>T	ENSP00000436804.2:n.*837C>T
ENST00000524377.7:c.2245C>T MANE Select	ENSP00000431418.1:p.Pro749Ser
ENST00000531606.2:c.304C>T
ENST00000674537.1:c.2065C>T	ENSP00000502725.1:p.Pro689Ser
ENST00000358660.3:c.2236C>T	ENSP00000351486.3:p.Pro746Ser
ENST00000368196.7:c.2227C>T	ENSP00000357179.3:p.Pro743Ser
ENST00000392302.6:c.2137C>T	ENSP00000376120.2:p.Pro713Ser
ENST00000497019.6:c.*837C>T	ENSP00000436804.1:n.*837C>T
ENST00000524377.5:c.2245C>T	ENSP00000431418.1:p.Pro749Ser
ENST00000530298.5:n.2698C>T
ENST00000531606.1:n.288C>T
NM_001007792.1:c.2137C>T , LRG_261t1:c.2137C>T	NP_001007793.1:p.Pro713Ser
NM_001012331.1:c.2227C>T , LRG_261t2:c.2227C>T	NP_001012331.1:p.Pro743Ser
NM_002529.3:c.2245C>T , LRG_261t3:c.2245C>T	NP_002520.2:p.Pro749Ser
NM_001012331.2:c.2227C>T	NP_001012331.1:p.Pro743Ser
NM_002529.4:c.2245C>T MANE Select	NP_002520.2:p.Pro749Ser