Canonical Allele Identifier: CA406804783
Gene: NTF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061397A>G , CM000681.2:g.49061397A>G GRCh38
NC_000019.9:g.49564654A>G , CM000681.1:g.49564654A>G GRCh37
NC_000019.8:g.54256466A>G NCBI36
NG_016289.1:g.7471T>C

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.601T>C NP_006170.1:p.Cys201Arg
XM_005258962.2:c.601T>C XP_005259019.1:p.Cys201Arg
XM_006723232.2:c.601T>C XP_006723295.1:p.Cys201Arg
XM_011527008.1:c.631T>C XP_011525310.1:p.Cys211Arg
XM_011527009.1:c.601T>C XP_011525311.1:p.Cys201Arg
XM_011527010.1:c.601T>C XP_011525312.1:p.Cys201Arg
XM_005258962.3:c.601T>C XP_005259019.1:p.Cys201Arg
XM_006723232.3:c.601T>C XP_006723295.1:p.Cys201Arg
XM_011527008.2:c.631T>C XP_011525310.1:p.Cys211Arg
XM_011527009.2:c.601T>C XP_011525311.1:p.Cys201Arg
XM_011527010.2:c.601T>C XP_011525312.1:p.Cys201Arg
XR_001753693.1:n.646T>C
XR_001753694.1:n.646T>C
ENST00000593537.1:n.601T>C ENSP00000469455.1:p.Cys201Arg
ENST00000599795.5:c.243+358T>C ENSP00000470689.1:p.=