Canonical Allele Identifier: CA406804741

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564644A>T (hg19) ; chr19:g.49061387A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061387A>T , CM000681.2:g.49061387A>T	GRCh38
NC_000019.9:g.49564644A>T , CM000681.1:g.49564644A>T	GRCh37
NC_000019.8:g.54256456A>T	NCBI36
NG_016289.1:g.7481T>A

Transcript Alleles

HGVS	Amino-acid change
NM_006179.4:c.611T>A	NP_006170.1:p.Leu204His
XM_005258962.2:c.611T>A	XP_005259019.1:p.Leu204His
XM_006723232.2:c.611T>A	XP_006723295.1:p.Leu204His
XM_011527008.1:c.641T>A	XP_011525310.1:p.Leu214His
XM_011527009.1:c.611T>A	XP_011525311.1:p.Leu204His
XM_011527010.1:c.611T>A	XP_011525312.1:p.Leu204His
XM_005258962.3:c.611T>A	XP_005259019.1:p.Leu204His
XM_006723232.3:c.611T>A	XP_006723295.1:p.Leu204His
XM_011527008.2:c.641T>A	XP_011525310.1:p.Leu214His
XM_011527009.2:c.611T>A	XP_011525311.1:p.Leu204His
XM_011527010.2:c.611T>A	XP_011525312.1:p.Leu204His
XR_001753693.1:n.656T>A
XR_001753694.1:n.656T>A
ENST00000593537.1:n.611T>A	ENSP00000469455.1:p.Leu204His
ENST00000599795.5:c.243+368T>A	ENSP00000470689.1:p.=