Canonical Allele Identifier: CA342939873

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156879264-G-A
• COSMIC: COSM5905422 ; COSM5905423
• MyVariant Identifiers: chr1:g.156849056G>A (hg19) ; chr1:g.156879264G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879264G>A , CM000663.2:g.156879264G>A	GRCh38
NC_000001.10:g.156849056G>A , CM000663.1:g.156849056G>A	GRCh37
NC_000001.9:g.155115680G>A	NCBI36
NG_007493.1:g.68515G>A , LRG_261:g.68515G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1768G>A	ENSP00000502725.1:p.Asp590Asn
ENST00000392302.7:c.1768G>A	ENSP00000376120.3:p.Asp590Asn
ENST00000497019.7:c.*540G>A	ENSP00000436804.2:n.*540G>A
ENST00000524377.7:c.1948G>A MANE Select	ENSP00000431418.1:p.Asp650Asn
ENST00000674537.1:c.1768G>A	ENSP00000502725.1:p.Asp590Asn
ENST00000358660.3:c.1939G>A	ENSP00000351486.3:p.Asp647Asn
ENST00000368196.7:c.1930G>A	ENSP00000357179.3:p.Asp644Asn
ENST00000392302.6:c.1840G>A	ENSP00000376120.2:p.Asp614Asn
ENST00000497019.6:c.*540G>A	ENSP00000436804.1:n.*540G>A
ENST00000524377.5:c.1948G>A	ENSP00000431418.1:p.Asp650Asn
ENST00000530298.5:n.2401G>A
NM_001007792.1:c.1840G>A , LRG_261t1:c.1840G>A	NP_001007793.1:p.Asp614Asn
NM_001012331.1:c.1930G>A , LRG_261t2:c.1930G>A	NP_001012331.1:p.Asp644Asn
NM_002529.3:c.1948G>A , LRG_261t3:c.1948G>A	NP_002520.2:p.Asp650Asn
NM_001012331.2:c.1930G>A	NP_001012331.1:p.Asp644Asn
NM_002529.4:c.1948G>A MANE Select	NP_002520.2:p.Asp650Asn