Canonical Allele Identifier: CA342937196

Gene: NTRK1

Linked Data

• dbSNP Id: rs1373141980
• gnomAD v2: 1-156845314-C-T
• MyVariant Identifiers: chr1:g.156845314C>T (hg19) ; chr1:g.156875522C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875522C>T , CM000663.2:g.156875522C>T	GRCh38
NC_000001.10:g.156845314C>T , CM000663.1:g.156845314C>T	GRCh37
NC_000001.9:g.155111938C>T	NCBI36
NG_007493.1:g.64773C>T , LRG_261:g.64773C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1177C>T	ENSP00000502725.1:p.Pro393Ser
ENST00000392302.7:c.1177C>T	ENSP00000376120.3:p.Pro393Ser
ENST00000497019.7:c.1044C>T	ENSP00000436804.2:p.Ala348=
ENST00000524377.7:c.1357C>T MANE Select	ENSP00000431418.1:p.Pro453Ser
ENST00000674537.1:c.1177C>T	ENSP00000502725.1:p.Pro393Ser
ENST00000358660.3:c.1339C>T	ENSP00000351486.3:p.Pro447Ser
ENST00000368196.7:c.1339C>T	ENSP00000357179.3:p.Pro447Ser
ENST00000392302.6:c.1249C>T	ENSP00000376120.2:p.Pro417Ser
ENST00000497019.6:c.1116C>T	ENSP00000436804.1:p.Ala372=
ENST00000524377.5:c.1357C>T	ENSP00000431418.1:p.Pro453Ser
ENST00000530298.5:n.1397C>T
ENST00000534682.1:n.580C>T
NM_001007792.1:c.1249C>T , LRG_261t1:c.1249C>T	NP_001007793.1:p.Pro417Ser
NM_001012331.1:c.1339C>T , LRG_261t2:c.1339C>T	NP_001012331.1:p.Pro447Ser
NM_002529.3:c.1357C>T , LRG_261t3:c.1357C>T	NP_002520.2:p.Pro453Ser
NM_001012331.2:c.1339C>T	NP_001012331.1:p.Pro447Ser
NM_002529.4:c.1357C>T MANE Select	NP_002520.2:p.Pro453Ser