Canonical Allele Identifier: CA31100859

Gene: NTRK1

Linked Data

• dbSNP Id: rs996948714
• gnomAD v4: 1-156860876-A-C
• MyVariant Identifiers: chr1:g.156830668A>C (hg19) ; chr1:g.156860876A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860876A>C , CM000663.2:g.156860876A>C	GRCh38
NC_000001.10:g.156830668A>C , CM000663.1:g.156830668A>C	GRCh37
NC_000001.9:g.155097292A>C	NCBI36
NG_007493.1:g.50127A>C , LRG_261:g.50127A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3478A>C	ENSP00000502725.1:n.51-3478A>C
ENST00000392302.7:c.51-3478A>C	ENSP00000376120.3:n.51-3478A>C
ENST00000497019.7:c.51-3478A>C	ENSP00000436804.2:n.51-3478A>C
ENST00000524377.7:c.-59A>C MANE Select	ENSP00000431418.1:n.-59A>C
ENST00000674537.1:c.51-3478A>C	ENSP00000502725.1:n.51-3478A>C
ENST00000368196.7:c.-59A>C	ENSP00000357179.3:n.-59A>C
ENST00000392302.6:c.123-3478A>C	ENSP00000376120.2:n.123-3478A>C
ENST00000489021.6:n.313-12757A>C
ENST00000497019.6:c.123-3478A>C	ENSP00000436804.1:n.123-3478A>C
ENST00000530298.5:n.271-3478A>C
NM_001007792.1:c.123-3478A>C , LRG_261t1:c.123-3478A>C	NP_001007793.1:n.123-3478A>C
NM_001012331.2:c.-59A>C	NP_001012331.1:n.-59A>C
NM_002529.4:c.-59A>C MANE Select	NP_002520.2:n.-59A>C