Canonical Allele Identifier: CA421140441

Gene: NTRK1

Linked Data

• dbSNP Id: rs1057521447
• MyVariant Identifiers: chr1:g.156849811G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880019G>C , CM000663.2:g.156880019G>C	GRCh38
NC_000001.10:g.156849811G>C , CM000663.1:g.156849811G>C	GRCh37
NC_000001.9:g.155116435G>C	NCBI36
NG_007493.1:g.69270G>C , LRG_261:g.69270G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1887G>C	ENSP00000502725.1:p.Leu629=
ENST00000392302.7:c.1887G>C	ENSP00000376120.3:p.Leu629=
ENST00000497019.7:c.*659G>C	ENSP00000436804.2:n.*659G>C
ENST00000524377.7:c.2067G>C MANE Select	ENSP00000431418.1:p.Leu689=
ENST00000531606.2:c.35G>C
ENST00000674537.1:c.1887G>C	ENSP00000502725.1:p.Leu629=
ENST00000358660.3:c.2058G>C	ENSP00000351486.3:p.Leu686=
ENST00000368196.7:c.2049G>C	ENSP00000357179.3:p.Leu683=
ENST00000392302.6:c.1959G>C	ENSP00000376120.2:p.Leu653=
ENST00000497019.6:c.*659G>C	ENSP00000436804.1:n.*659G>C
ENST00000524377.5:c.2067G>C	ENSP00000431418.1:p.Leu689=
ENST00000530298.5:n.2520G>C
ENST00000531606.1:n.19G>C
NM_001007792.1:c.1959G>C , LRG_261t1:c.1959G>C	NP_001007793.1:p.Leu653=
NM_001012331.1:c.2049G>C , LRG_261t2:c.2049G>C	NP_001012331.1:p.Leu683=
NM_002529.3:c.2067G>C , LRG_261t3:c.2067G>C	NP_002520.2:p.Leu689=
NM_001012331.2:c.2049G>C	NP_001012331.1:p.Leu683=
NM_002529.4:c.2067G>C MANE Select	NP_002520.2:p.Leu689=