Canonical Allele Identifier: CA342939489

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156848949G>A (hg19) ; chr1:g.156879157G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879157G>A , CM000663.2:g.156879157G>A	GRCh38
NC_000001.10:g.156848949G>A , CM000663.1:g.156848949G>A	GRCh37
NC_000001.9:g.155115573G>A	NCBI36
NG_007493.1:g.68408G>A , LRG_261:g.68408G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1661G>A	ENSP00000502725.1:p.Gly554Glu
ENST00000392302.7:c.1661G>A	ENSP00000376120.3:p.Gly554Glu
ENST00000497019.7:c.*433G>A	ENSP00000436804.2:n.*433G>A
ENST00000524377.7:c.1841G>A MANE Select	ENSP00000431418.1:p.Gly614Glu
ENST00000674537.1:c.1661G>A	ENSP00000502725.1:p.Gly554Glu
ENST00000358660.3:c.1832G>A	ENSP00000351486.3:p.Gly611Glu
ENST00000368196.7:c.1823G>A	ENSP00000357179.3:p.Gly608Glu
ENST00000392302.6:c.1733G>A	ENSP00000376120.2:p.Gly578Glu
ENST00000497019.6:c.*433G>A	ENSP00000436804.1:n.*433G>A
ENST00000524377.5:c.1841G>A	ENSP00000431418.1:p.Gly614Glu
ENST00000530298.5:n.2294G>A
NM_001007792.1:c.1733G>A , LRG_261t1:c.1733G>A	NP_001007793.1:p.Gly578Glu
NM_001012331.1:c.1823G>A , LRG_261t2:c.1823G>A	NP_001012331.1:p.Gly608Glu
NM_002529.3:c.1841G>A , LRG_261t3:c.1841G>A	NP_002520.2:p.Gly614Glu
NM_001012331.2:c.1823G>A	NP_001012331.1:p.Gly608Glu
NM_002529.4:c.1841G>A MANE Select	NP_002520.2:p.Gly614Glu