Canonical Allele Identifier: CA342938450

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102919232
• MyVariant Identifiers: chr1:g.156846224G>C (hg19) ; chr1:g.156876432G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876432G>C , CM000663.2:g.156876432G>C	GRCh38
NC_000001.10:g.156846224G>C , CM000663.1:g.156846224G>C	GRCh37
NC_000001.9:g.155112848G>C	NCBI36
NG_007493.1:g.65683G>C , LRG_261:g.65683G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1485G>C	ENSP00000502725.1:p.Gln495His
ENST00000392302.7:c.1485G>C	ENSP00000376120.3:p.Gln495His
ENST00000497019.7:c.*257G>C	ENSP00000436804.2:n.*257G>C
ENST00000524377.7:c.1665G>C MANE Select	ENSP00000431418.1:p.Gln555His
ENST00000674537.1:c.1485G>C	ENSP00000502725.1:p.Gln495His
ENST00000358660.3:c.1656G>C	ENSP00000351486.3:p.Gln552His
ENST00000368196.7:c.1647G>C	ENSP00000357179.3:p.Gln549His
ENST00000392302.6:c.1557G>C	ENSP00000376120.2:p.Gln519His
ENST00000497019.6:c.*257G>C	ENSP00000436804.1:n.*257G>C
ENST00000524377.5:c.1665G>C	ENSP00000431418.1:p.Gln555His
ENST00000530298.5:n.2118G>C
NM_001007792.1:c.1557G>C , LRG_261t1:c.1557G>C	NP_001007793.1:p.Gln519His
NM_001012331.1:c.1647G>C , LRG_261t2:c.1647G>C	NP_001012331.1:p.Gln549His
NM_002529.3:c.1665G>C , LRG_261t3:c.1665G>C	NP_002520.2:p.Gln555His
NM_001012331.2:c.1647G>C	NP_001012331.1:p.Gln549His
NM_002529.4:c.1665G>C MANE Select	NP_002520.2:p.Gln555His