Canonical Allele Identifier: CA406804778
Gene: NTF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061396C>G , CM000681.2:g.49061396C>G GRCh38
NC_000019.9:g.49564653C>G , CM000681.1:g.49564653C>G GRCh37
NC_000019.8:g.54256465C>G NCBI36
NG_016289.1:g.7472G>C

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.602G>C NP_006170.1:p.Cys201Ser
XM_005258962.2:c.602G>C XP_005259019.1:p.Cys201Ser
XM_006723232.2:c.602G>C XP_006723295.1:p.Cys201Ser
XM_011527008.1:c.632G>C XP_011525310.1:p.Cys211Ser
XM_011527009.1:c.602G>C XP_011525311.1:p.Cys201Ser
XM_011527010.1:c.602G>C XP_011525312.1:p.Cys201Ser
XM_005258962.3:c.602G>C XP_005259019.1:p.Cys201Ser
XM_006723232.3:c.602G>C XP_006723295.1:p.Cys201Ser
XM_011527008.2:c.632G>C XP_011525310.1:p.Cys211Ser
XM_011527009.2:c.602G>C XP_011525311.1:p.Cys201Ser
XM_011527010.2:c.602G>C XP_011525312.1:p.Cys201Ser
XR_001753693.1:n.647G>C
XR_001753694.1:n.647G>C
ENST00000593537.1:n.602G>C ENSP00000469455.1:p.Cys201Ser
ENST00000599795.5:c.243+359G>C ENSP00000470689.1:p.=