Canonical Allele Identifier: CA342938395

Gene: NTRK1

Linked Data

• dbSNP Id: rs1647912850
• MyVariant Identifiers: chr1:g.156846201G>C (hg19) ; chr1:g.156876409G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876409G>C , CM000663.2:g.156876409G>C	GRCh38
NC_000001.10:g.156846201G>C , CM000663.1:g.156846201G>C	GRCh37
NC_000001.9:g.155112825G>C	NCBI36
NG_007493.1:g.65660G>C , LRG_261:g.65660G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1462G>C	ENSP00000502725.1:p.Glu488Gln
ENST00000392302.7:c.1462G>C	ENSP00000376120.3:p.Glu488Gln
ENST00000497019.7:c.*234G>C	ENSP00000436804.2:n.*234G>C
ENST00000524377.7:c.1642G>C MANE Select	ENSP00000431418.1:p.Glu548Gln
ENST00000674537.1:c.1462G>C	ENSP00000502725.1:p.Glu488Gln
ENST00000358660.3:c.1633G>C	ENSP00000351486.3:p.Glu545Gln
ENST00000368196.7:c.1624G>C	ENSP00000357179.3:p.Glu542Gln
ENST00000392302.6:c.1534G>C	ENSP00000376120.2:p.Glu512Gln
ENST00000497019.6:c.*234G>C	ENSP00000436804.1:n.*234G>C
ENST00000524377.5:c.1642G>C	ENSP00000431418.1:p.Glu548Gln
ENST00000530298.5:n.2095G>C
NM_001007792.1:c.1534G>C , LRG_261t1:c.1534G>C	NP_001007793.1:p.Glu512Gln
NM_001012331.1:c.1624G>C , LRG_261t2:c.1624G>C	NP_001012331.1:p.Glu542Gln
NM_002529.3:c.1642G>C , LRG_261t3:c.1642G>C	NP_002520.2:p.Glu548Gln
NM_001012331.2:c.1624G>C	NP_001012331.1:p.Glu542Gln
NM_002529.4:c.1642G>C MANE Select	NP_002520.2:p.Glu548Gln