Canonical Allele Identifier: CA2840289880

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061346A>T , CM000681.2:g.49061346A>T	GRCh38
NC_000019.9:g.49564603A>T , CM000681.1:g.49564603A>T	GRCh37
NC_000019.8:g.54256415A>T	NCBI36
NG_016289.1:g.7522T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.*19T>A MANE Select	ENSP00000469455.1:n.*19T>A
ENST00000594938.2:c.*19T>A	ENSP00000512387.1:n.*19T>A
ENST00000595857.6:c.*19T>A	ENSP00000471508.2:n.*19T>A
ENST00000696088.1:c.*19T>A	ENSP00000512384.1:n.*19T>A
ENST00000696089.1:c.*19T>A	ENSP00000512385.1:n.*19T>A
ENST00000696090.1:c.*19T>A	ENSP00000512386.1:n.*19T>A
ENST00000696091.1:c.*19T>A	ENSP00000512388.1:n.*19T>A
ENST00000593537.1:c.652T>A	ENSP00000469455.1:n.652T>A
ENST00000599795.5:c.243+409T>A	ENSP00000470689.1:n.243+409T>A
NM_006179.4:c.*19T>A	NP_006170.1:n.*19T>A
XM_005258962.2:c.*19T>A	XP_005259019.1:n.*19T>A
XM_006723232.2:c.*19T>A	XP_006723295.1:n.*19T>A
XM_011527008.1:c.*19T>A	XP_011525310.1:n.*19T>A
XM_011527009.1:c.*19T>A	XP_011525311.1:n.*19T>A
XM_011527010.1:c.*19T>A	XP_011525312.1:n.*19T>A
XM_005258962.3:c.*19T>A	XP_005259019.1:n.*19T>A
XM_006723232.3:c.*19T>A	XP_006723295.1:n.*19T>A
XM_011527008.2:c.*19T>A	XP_011525310.1:n.*19T>A
XM_011527009.2:c.*19T>A	XP_011525311.1:n.*19T>A
XM_011527010.2:c.*19T>A	XP_011525312.1:n.*19T>A
XR_001753693.1:n.697T>A
XR_001753694.1:n.697T>A
NM_001395489.1:c.*19T>A	NP_001382418.1:n.*19T>A
NM_006179.5:c.*19T>A MANE Select	NP_006170.1:n.*19T>A