Canonical Allele Identifier: CA342937952

Gene: NTRK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876128G>C , CM000663.2:g.156876128G>C	GRCh38
NC_000001.10:g.156845920G>C , CM000663.1:g.156845920G>C	GRCh37
NC_000001.9:g.155112544G>C	NCBI36
NG_007493.1:g.65379G>C , LRG_261:g.65379G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1370G>C	ENSP00000502725.1:p.Gly457Ala
ENST00000392302.7:c.1370G>C	ENSP00000376120.3:p.Gly457Ala
ENST00000497019.7:c.*142G>C	ENSP00000436804.2:n.*142G>C
ENST00000524377.7:c.1550G>C MANE Select	ENSP00000431418.1:p.Gly517Ala
ENST00000674537.1:c.1370G>C	ENSP00000502725.1:p.Gly457Ala
ENST00000358660.3:c.1541G>C	ENSP00000351486.3:p.Gly514Ala
ENST00000368196.7:c.1532G>C	ENSP00000357179.3:p.Gly511Ala
ENST00000392302.6:c.1442G>C	ENSP00000376120.2:p.Gly481Ala
ENST00000497019.6:c.*142G>C	ENSP00000436804.1:n.*142G>C
ENST00000524377.5:c.1550G>C	ENSP00000431418.1:p.Gly517Ala
ENST00000530298.5:n.2003G>C
ENST00000534682.1:n.773G>C
NM_001007792.1:c.1442G>C , LRG_261t1:c.1442G>C	NP_001007793.1:p.Gly481Ala
NM_001012331.1:c.1532G>C , LRG_261t2:c.1532G>C	NP_001012331.1:p.Gly511Ala
NM_002529.3:c.1550G>C , LRG_261t3:c.1550G>C	NP_002520.2:p.Gly517Ala
NM_001012331.2:c.1532G>C	NP_001012331.1:p.Gly511Ala
NM_002529.4:c.1550G>C MANE Select	NP_002520.2:p.Gly517Ala