Canonical Allele Identifier: CA406804727
Gene: NTF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061382G>C , CM000681.2:g.49061382G>C GRCh38
NC_000019.9:g.49564639G>C , CM000681.1:g.49564639G>C GRCh37
NC_000019.8:g.54256451G>C NCBI36
NG_016289.1:g.7486C>G

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.616C>G NP_006170.1:p.Arg206Gly
XM_005258962.2:c.616C>G XP_005259019.1:p.Arg206Gly
XM_006723232.2:c.616C>G XP_006723295.1:p.Arg206Gly
XM_011527008.1:c.646C>G XP_011525310.1:p.Arg216Gly
XM_011527009.1:c.616C>G XP_011525311.1:p.Arg206Gly
XM_011527010.1:c.616C>G XP_011525312.1:p.Arg206Gly
XM_005258962.3:c.616C>G XP_005259019.1:p.Arg206Gly
XM_006723232.3:c.616C>G XP_006723295.1:p.Arg206Gly
XM_011527008.2:c.646C>G XP_011525310.1:p.Arg216Gly
XM_011527009.2:c.616C>G XP_011525311.1:p.Arg206Gly
XM_011527010.2:c.616C>G XP_011525312.1:p.Arg206Gly
XR_001753693.1:n.661C>G
XR_001753694.1:n.661C>G
ENST00000593537.1:n.616C>G ENSP00000469455.1:p.Arg206Gly
ENST00000599795.5:c.243+373C>G ENSP00000470689.1:p.=