Canonical Allele Identifier: CA1169575

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880092G>A , CM000663.2:g.156880092G>A	GRCh38
NC_000001.10:g.156849884G>A , CM000663.1:g.156849884G>A	GRCh37
NC_000001.9:g.155116508G>A	NCBI36
NG_007493.1:g.69343G>A , LRG_261:g.69343G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.2140G>A MANE Select	NP_002520.2:p.Gly714Ser
ENST00000524377.7:c.2140G>A MANE Select	ENSP00000431418.1:p.Gly714Ser
NM_001007792.1:c.2032G>A , LRG_261t1:c.2032G>A	NP_001007793.1:p.Gly678Ser
NM_001012331.1:c.2122G>A , LRG_261t2:c.2122G>A	NP_001012331.1:p.Gly708Ser
NM_001012331.2:c.2122G>A	NP_001012331.1:p.Gly708Ser
NM_002529.3:c.2140G>A , LRG_261t3:c.2140G>A	NP_002520.2:p.Gly714Ser
ENST00000358660.3:c.2131G>A	ENSP00000351486.3:p.Gly711Ser
ENST00000368196.7:c.2122G>A	ENSP00000357179.3:p.Gly708Ser
ENST00000392302.6:c.2032G>A	ENSP00000376120.2:p.Gly678Ser
ENST00000392302.7:c.1960G>A	ENSP00000376120.3:p.Gly654Ser
ENST00000497019.6:c.*732G>A	ENSP00000436804.1:n.*732G>A
ENST00000497019.7:c.*732G>A	ENSP00000436804.2:n.*732G>A
ENST00000524377.5:c.2140G>A	ENSP00000431418.1:p.Gly714Ser
ENST00000530298.5:n.2593G>A
ENST00000531606.1:n.92G>A
ENST00000531606.2:c.108G>A
ENST00000674537.1:c.1960G>A	ENSP00000502725.1:p.Gly654Ser
ENST00000674537.2:c.1960G>A	ENSP00000502725.1:p.Gly654Ser