Canonical Allele Identifier: CA374009649

Gene: NTRK2

Linked Data

• dbSNP Id: rs2289657
• gnomAD v4: 9-84948545-C-G
• MyVariant Identifiers: chr9:g.87563460C>G (hg19) ; chr9:g.84948545C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84948545C>G , CM000671.2:g.84948545C>G	GRCh38
NC_000009.11:g.87563460C>G , CM000671.1:g.87563460C>G	GRCh37
NC_000009.10:g.86753280C>G	NCBI36
NG_012201.2:g.284995C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000323115.11:c.1764C>G	ENSP00000314586.5:p.Ile588Met
ENST00000685095.1:n.2334C>G
ENST00000685463.1:n.2465C>G
ENST00000686259.1:c.1800C>G	ENSP00000509743.1:p.Ile600Met
ENST00000686324.1:c.1848C>G	ENSP00000510134.1:p.Ile616Met
ENST00000686332.1:n.2878C>G
ENST00000686496.1:c.1800C>G	ENSP00000510060.1:p.Ile600Met
ENST00000687386.1:c.1800C>G	ENSP00000508723.1:p.Ile600Met
ENST00000688333.1:n.2733C>G
ENST00000688978.1:n.519C>G
ENST00000689301.1:c.1332C>G	ENSP00000510766.1:p.Ile444Met
ENST00000690882.1:n.2465C>G
ENST00000691788.1:c.1800C>G	ENSP00000509401.1:p.Ile600Met
ENST00000692181.1:c.1800C>G	ENSP00000510619.1:p.Ile600Met
ENST00000692473.1:c.1380C>G	ENSP00000509020.1:p.Ile460Met
ENST00000277120.8:c.1848C>G MANE Select	ENSP00000277120.3:p.Ile616Met
ENST00000323115.10:c.1800C>G	ENSP00000314586.4:p.Ile600Met
ENST00000376213.6:c.1800C>G	ENSP00000365386.1:p.Ile600Met
ENST00000277120.7:c.1848C>G	ENSP00000277120.3:p.Ile616Met
ENST00000323115.8:c.1800C>G	ENSP00000314586.4:p.Ile600Met
ENST00000376213.5:c.1800C>G	ENSP00000365386.1:p.Ile600Met
ENST00000376214.5:c.1848C>G	ENSP00000365387.1:p.Ile616Met
NM_001018064.2:c.1800C>G	NP_001018074.1:p.Ile600Met
NM_006180.4:c.1848C>G	NP_006171.2:p.Ile616Met
XM_005252001.1:c.1848C>G	XP_005252058.1:p.Ile616Met
XM_005252003.1:c.1848C>G	XP_005252060.1:p.Ile616Met
XM_005252004.1:c.1848C>G	XP_005252061.1:p.Ile616Met
XM_011518718.1:c.1800C>G	XP_011517020.1:p.Ile600Met
XM_011518719.1:c.1800C>G	XP_011517021.1:p.Ile600Met
XM_005252001.3:c.1848C>G	XP_005252058.1:p.Ile616Met
XM_005252003.3:c.1848C>G	XP_005252060.1:p.Ile616Met
XM_005252004.2:c.1848C>G	XP_005252061.1:p.Ile616Met
XM_011518718.3:c.1800C>G	XP_011517020.1:p.Ile600Met
XM_017014751.2:c.1848C>G	XP_016870240.1:p.Ile616Met
XM_017014752.1:c.1800C>G	XP_016870241.1:p.Ile600Met
XM_017014753.2:c.1800C>G	XP_016870242.1:p.Ile600Met
XM_017014754.1:c.1800C>G	XP_016870243.1:p.Ile600Met
NM_001018064.3:c.1800C>G	NP_001018074.1:p.Ile600Met
NM_001369532.1:c.1800C>G	NP_001356461.1:p.Ile600Met
NM_001369533.1:c.1800C>G	NP_001356462.1:p.Ile600Met
NM_001369534.1:c.1764C>G	NP_001356463.1:p.Ile588Met
NM_001369535.1:c.1332C>G	NP_001356464.1:p.Ile444Met
NM_001369536.1:c.1380C>G	NP_001356465.1:p.Ile460Met
NM_006180.5:c.1848C>G	NP_006171.2:p.Ile616Met
NM_006180.6:c.1848C>G MANE Select	NP_006171.2:p.Ile616Met