Canonical Allele Identifier: CA2648465199

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156879014-G-GGCCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879015_156879016insCCCCCAG , CM000663.2:g.156879015_156879016insCCCCCAG	GRCh38
NC_000001.10:g.156848807_156848808insCCCCCAG , CM000663.1:g.156848807_156848808insCCCCCAG	GRCh37
NC_000001.9:g.155115431_155115432insCCCCCAG	NCBI36
NG_007493.1:g.68266_68267insCCCCCAG , LRG_261:g.68266_68267insCCCCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1626-107_1626-106insCCCCCAG	ENSP00000502725.1:n.1626-107_1626-106insCCCCCAG
ENST00000392302.7:c.1626-107_1626-106insCCCCCAG	ENSP00000376120.3:n.1626-107_1626-106insCCCCCAG
ENST00000497019.7:c.*398-107_*398-106insCCCCCAG	ENSP00000436804.2:n.*398-107_*398-106insCCCCCAG
ENST00000524377.7:c.1806-107_1806-106insCCCCCAG MANE Select	ENSP00000431418.1:n.1806-107_1806-106insCCCCCAG
ENST00000674537.1:c.1626-107_1626-106insCCCCCAG	ENSP00000502725.1:n.1626-107_1626-106insCCCCCAG
ENST00000358660.3:c.1797-107_1797-106insCCCCCAG	ENSP00000351486.3:n.1797-107_1797-106insCCCCCAG
ENST00000368196.7:c.1788-107_1788-106insCCCCCAG	ENSP00000357179.3:n.1788-107_1788-106insCCCCCAG
ENST00000392302.6:c.1698-107_1698-106insCCCCCAG	ENSP00000376120.2:n.1698-107_1698-106insCCCCCAG
ENST00000497019.6:c.*398-107_*398-106insCCCCCAG	ENSP00000436804.1:n.*398-107_*398-106insCCCCCAG
ENST00000524377.5:c.1806-107_1806-106insCCCCCAG	ENSP00000431418.1:n.1806-107_1806-106insCCCCCAG
ENST00000530298.5:n.2259-107_2259-106insCCCCCAG
NM_001007792.1:c.1698-107_1698-106insCCCCCAG , LRG_261t1:c.1698-107_1698-106insCCCCCAG	NP_001007793.1:n.1698-107_1698-106insCCCCCAG
NM_001012331.1:c.1788-107_1788-106insCCCCCAG , LRG_261t2:c.1788-107_1788-106insCCCCCAG	NP_001012331.1:n.1788-107_1788-106insCCCCCAG
NM_002529.3:c.1806-107_1806-106insCCCCCAG , LRG_261t3:c.1806-107_1806-106insCCCCCAG	NP_002520.2:n.1806-107_1806-106insCCCCCAG
NM_001012331.2:c.1788-107_1788-106insCCCCCAG	NP_001012331.1:n.1788-107_1788-106insCCCCCAG
NM_002529.4:c.1806-107_1806-106insCCCCCAG MANE Select	NP_002520.2:n.1806-107_1806-106insCCCCCAG