Canonical Allele Identifier: CA2840056862

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876404_156876405insCTCGGACGCCTCCTTCAGTGCCTG , CM000663.2:g.156876404_156876405insCTCGGACGCCTCCTTCAGTGCCTG	GRCh38
NC_000001.10:g.156846196_156846197insCTCGGACGCCTCCTTCAGTGCCTG , CM000663.1:g.156846196_156846197insCTCGGACGCCTCCTTCAGTGCCTG	GRCh37
NC_000001.9:g.155112820_155112821insCTCGGACGCCTCCTTCAGTGCCTG	NCBI36
NG_007493.1:g.65655_65656insCTCGGACGCCTCCTTCAGTGCCTG , LRG_261:g.65655_65656insCTCGGACGCCTCCTTCAGTGCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1457_1458insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000502725.1:p.Leu486_Lys487insSerAspAlaSerPheSerAlaTrp
ENST00000392302.7:c.1457_1458insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000376120.3:p.Leu486_Lys487insSerAspAlaSerPheSerAlaTrp
ENST00000497019.7:c.*229_*230insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000436804.2:n.*229_*230insCTCGGACGCCTCCTTCAGTGCCTG
ENST00000524377.7:c.1637_1638insCTCGGACGCCTCCTTCAGTGCCTG MANE Select	ENSP00000431418.1:p.Leu546_Lys547insSerAspAlaSerPheSerAlaTrp
ENST00000674537.1:c.1457_1458insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000502725.1:p.Leu486_Lys487insSerAspAlaSerPheSerAlaTrp
ENST00000358660.3:c.1628_1629insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000351486.3:p.Leu543_Lys544insSerAspAlaSerPheSerAlaTrp
ENST00000368196.7:c.1619_1620insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000357179.3:p.Leu540_Lys541insSerAspAlaSerPheSerAlaTrp
ENST00000392302.6:c.1529_1530insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000376120.2:p.Leu510_Lys511insSerAspAlaSerPheSerAlaTrp
ENST00000497019.6:c.*229_*230insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000436804.1:n.*229_*230insCTCGGACGCCTCCTTCAGTGCCTG
ENST00000524377.5:c.1637_1638insCTCGGACGCCTCCTTCAGTGCCTG	ENSP00000431418.1:p.Leu546_Lys547insSerAspAlaSerPheSerAlaTrp
ENST00000530298.5:n.2090_2091insCTCGGACGCCTCCTTCAGTGCCTG
NM_001007792.1:c.1529_1530insCTCGGACGCCTCCTTCAGTGCCTG , LRG_261t1:c.1529_1530insCTCGGACGCCTCCTTCAGTGCCTG	NP_001007793.1:p.Leu510_Lys511insSerAspAlaSerPheSerAlaTrp
NM_001012331.1:c.1619_1620insCTCGGACGCCTCCTTCAGTGCCTG , LRG_261t2:c.1619_1620insCTCGGACGCCTCCTTCAGTGCCTG	NP_001012331.1:p.Leu540_Lys541insSerAspAlaSerPheSerAlaTrp
NM_002529.3:c.1637_1638insCTCGGACGCCTCCTTCAGTGCCTG , LRG_261t3:c.1637_1638insCTCGGACGCCTCCTTCAGTGCCTG	NP_002520.2:p.Leu546_Lys547insSerAspAlaSerPheSerAlaTrp
NM_001012331.2:c.1619_1620insCTCGGACGCCTCCTTCAGTGCCTG	NP_001012331.1:p.Leu540_Lys541insSerAspAlaSerPheSerAlaTrp
NM_002529.4:c.1637_1638insCTCGGACGCCTCCTTCAGTGCCTG MANE Select	NP_002520.2:p.Leu546_Lys547insSerAspAlaSerPheSerAlaTrp