Canonical Allele Identifier: CA2648465692

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102926577
• gnomAD v4: 1-156879908-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879911del , CM000663.2:g.156879911del	GRCh38
NC_000001.10:g.156849703del , CM000663.1:g.156849703del	GRCh37
NC_000001.9:g.155116327del	NCBI36
NG_007493.1:g.69162del , LRG_261:g.69162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1867-88del	ENSP00000502725.1:n.1867-88del
ENST00000392302.7:c.1867-88del	ENSP00000376120.3:n.1867-88del
ENST00000497019.7:c.*639-88del	ENSP00000436804.2:n.*639-88del
ENST00000524377.7:c.2047-88del MANE Select	ENSP00000431418.1:n.2047-88del
ENST00000531606.2:c.15-88del
ENST00000674537.1:c.1867-88del	ENSP00000502725.1:n.1867-88del
ENST00000358660.3:c.2038-88del	ENSP00000351486.3:n.2038-88del
ENST00000368196.7:c.2029-88del	ENSP00000357179.3:n.2029-88del
ENST00000392302.6:c.1939-88del	ENSP00000376120.2:n.1939-88del
ENST00000497019.6:c.*639-88del	ENSP00000436804.1:n.*639-88del
ENST00000524377.5:c.2047-88del	ENSP00000431418.1:n.2047-88del
ENST00000530298.5:n.2500-88del
NM_001007792.1:c.1939-88del , LRG_261t1:c.1939-88del	NP_001007793.1:n.1939-88del
NM_001012331.1:c.2029-88del , LRG_261t2:c.2029-88del	NP_001012331.1:n.2029-88del
NM_002529.3:c.2047-88del , LRG_261t3:c.2047-88del	NP_002520.2:n.2047-88del
NM_001012331.2:c.2029-88del	NP_001012331.1:n.2029-88del
NM_002529.4:c.2047-88del MANE Select	NP_002520.2:n.2047-88del