Canonical Allele Identifier: CA2648465673
Gene: NTRK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156879895_156879897del , CM000663.2:g.156879895_156879897del GRCh38
NC_000001.10:g.156849687_156849689del , CM000663.1:g.156849687_156849689del GRCh37
NC_000001.9:g.155116311_155116313del NCBI36
NG_007493.1:g.69146_69148del , LRG_261:g.69146_69148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1867-104_1867-102del ENSP00000502725.1:n.1867-104_1867-102del
ENST00000392302.7:c.1867-104_1867-102del ENSP00000376120.3:n.1867-104_1867-102del
ENST00000497019.7:c.*639-104_*639-102del ENSP00000436804.2:n.*639-104_*639-102del
ENST00000524377.7:c.2047-104_2047-102del MANE Select ENSP00000431418.1:n.2047-104_2047-102del
ENST00000531606.2:c.15-104_15-102del
ENST00000674537.1:c.1867-104_1867-102del ENSP00000502725.1:n.1867-104_1867-102del
ENST00000358660.3:c.2038-104_2038-102del ENSP00000351486.3:n.2038-104_2038-102del
ENST00000368196.7:c.2029-104_2029-102del ENSP00000357179.3:n.2029-104_2029-102del
ENST00000392302.6:c.1939-104_1939-102del ENSP00000376120.2:n.1939-104_1939-102del
ENST00000497019.6:c.*639-104_*639-102del ENSP00000436804.1:n.*639-104_*639-102del
ENST00000524377.5:c.2047-104_2047-102del ENSP00000431418.1:n.2047-104_2047-102del
ENST00000530298.5:n.2500-104_2500-102del
NM_001007792.1:c.1939-104_1939-102del , LRG_261t1:c.1939-104_1939-102del NP_001007793.1:n.1939-104_1939-102del
NM_001012331.1:c.2029-104_2029-102del , LRG_261t2:c.2029-104_2029-102del NP_001012331.1:n.2029-104_2029-102del
NM_002529.3:c.2047-104_2047-102del , LRG_261t3:c.2047-104_2047-102del NP_002520.2:n.2047-104_2047-102del
NM_001012331.2:c.2029-104_2029-102del NP_001012331.1:n.2029-104_2029-102del
NM_002529.4:c.2047-104_2047-102del MANE Select NP_002520.2:n.2047-104_2047-102del