Canonical Allele Identifier: CA2340217569

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49062044_49062045delinsAG , CM000681.2:g.49062044_49062045delinsAG	GRCh38
NC_000019.9:g.49565301_49565302delinsAG , CM000681.1:g.49565301_49565302delinsAG	GRCh37
NC_000019.8:g.54257113_54257114delinsAG	NCBI36
NG_016289.1:g.6823_6824delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.-12-36_-12-35delinsCT MANE Select	ENSP00000469455.1:n.-12-36_-12-35delinsCT
ENST00000594938.2:c.-12-36_-12-35delinsCT	ENSP00000512387.1:n.-12-36_-12-35delinsCT
ENST00000595857.6:c.-12-36_-12-35delinsCT	ENSP00000471508.2:n.-12-36_-12-35delinsCT
ENST00000696088.1:c.-12-36_-12-35delinsCT	ENSP00000512384.1:n.-12-36_-12-35delinsCT
ENST00000696089.1:c.-12-36_-12-35delinsCT	ENSP00000512385.1:n.-12-36_-12-35delinsCT
ENST00000696090.1:c.-12-36_-12-35delinsCT	ENSP00000512386.1:n.-12-36_-12-35delinsCT
ENST00000696091.1:c.-12-36_-12-35delinsCT	ENSP00000512388.1:n.-12-36_-12-35delinsCT
ENST00000595857.5:c.-12-36_-12-35delinsCT	ENSP00000471508.1:n.-12-36_-12-35delinsCT
ENST00000599795.5:c.-12-36_-12-35delinsCT	ENSP00000470689.1:n.-12-36_-12-35delinsCT
NM_006179.4:c.-12-36_-12-35delinsCT	NP_006170.1:n.-12-36_-12-35delinsCT
XM_005258962.2:c.-12-36_-12-35delinsCT	XP_005259019.1:n.-12-36_-12-35delinsCT
XM_006723232.2:c.-12-36_-12-35delinsCT	XP_006723295.1:n.-12-36_-12-35delinsCT
XM_011527008.1:c.19-36_19-35delinsCT	XP_011525310.1:n.19-36_19-35delinsCT
XM_011527009.1:c.-12-36_-12-35delinsCT	XP_011525311.1:n.-12-36_-12-35delinsCT
XM_011527010.1:c.-12-36_-12-35delinsCT	XP_011525312.1:n.-12-36_-12-35delinsCT
XM_005258962.3:c.-12-36_-12-35delinsCT	XP_005259019.1:n.-12-36_-12-35delinsCT
XM_006723232.3:c.-12-36_-12-35delinsCT	XP_006723295.1:n.-12-36_-12-35delinsCT
XM_011527008.2:c.19-36_19-35delinsCT	XP_011525310.1:n.19-36_19-35delinsCT
XM_011527009.2:c.-12-36_-12-35delinsCT	XP_011525311.1:n.-12-36_-12-35delinsCT
XM_011527010.2:c.-12-36_-12-35delinsCT	XP_011525312.1:n.-12-36_-12-35delinsCT
XR_001753693.1:n.34-36_34-35delinsCT
XR_001753694.1:n.34-36_34-35delinsCT
NM_001395489.1:c.-12-36_-12-35delinsCT	NP_001382418.1:n.-12-36_-12-35delinsCT
NM_006179.5:c.-12-36_-12-35delinsCT MANE Select	NP_006170.1:n.-12-36_-12-35delinsCT