Canonical Allele Identifier: CA1139656371

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156880170C>A , CM000663.2:g.156880170C>A	GRCh38
NC_000001.10:g.156849962C>A , CM000663.1:g.156849962C>A	GRCh37
NC_000001.9:g.155116586C>A	NCBI36
NG_007493.1:g.69421C>A , LRG_261:g.69421C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.2205+13C>A MANE Select	NP_002520.2:n.2205+13C>A
ENST00000524377.7:c.2205+13C>A MANE Select	ENSP00000431418.1:n.2205+13C>A
NM_001007792.1:c.2097+13C>A , LRG_261t1:c.2097+13C>A	NP_001007793.1:n.2097+13C>A
NM_001012331.1:c.2187+13C>A , LRG_261t2:c.2187+13C>A	NP_001012331.1:n.2187+13C>A
NM_001012331.2:c.2187+13C>A	NP_001012331.1:n.2187+13C>A
NM_002529.3:c.2205+13C>A , LRG_261t3:c.2205+13C>A	NP_002520.2:n.2205+13C>A
ENST00000358660.3:c.2196+13C>A	ENSP00000351486.3:n.2196+13C>A
ENST00000368196.7:c.2187+13C>A	ENSP00000357179.3:n.2187+13C>A
ENST00000392302.6:c.2097+13C>A	ENSP00000376120.2:n.2097+13C>A
ENST00000392302.7:c.2025+13C>A	ENSP00000376120.3:n.2025+13C>A
ENST00000497019.6:c.*797+13C>A	ENSP00000436804.1:n.*797+13C>A
ENST00000497019.7:c.*797+13C>A	ENSP00000436804.2:n.*797+13C>A
ENST00000524377.5:c.2205+13C>A	ENSP00000431418.1:n.2205+13C>A
ENST00000530298.5:n.2658+13C>A
ENST00000531606.1:n.157+13C>A
ENST00000531606.2:c.173+13C>A
ENST00000674537.1:c.2025+13C>A	ENSP00000502725.1:n.2025+13C>A
ENST00000674537.2:c.2025+13C>A	ENSP00000502725.1:n.2025+13C>A