Canonical Allele Identifier: CA2574686971
Gene: SFXN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119147785del , CM000672.2:g.119147785del GRCh38
NC_000010.10:g.120907297del , CM000672.1:g.120907297del GRCh37
NC_000010.9:g.120897287del NCBI36
NG_033895.1:g.22913del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355697.7:c.813del MANE Select ENSP00000347924.2:p.Phe271LeufsTer17
ENST00000355697.6:c.813del ENSP00000347924.2:p.Phe271LeufsTer17
ENST00000369131.8:c.465del ENSP00000358127.4:p.Phe155LeufsTer17
ENST00000461438.5:n.842del
ENST00000466218.5:n.762del
ENST00000484960.5:n.143del
ENST00000490417.6:n.276del
NM_213649.1:c.813del NP_998814.1:p.Phe271LeufsTer17
NR_110305.1:n.831del
XM_005269525.3:c.786del XP_005269582.1:p.Phe262LeufsTer17
XM_005269526.1:c.465del XP_005269583.1:p.Phe155LeufsTer17
XM_005269527.1:c.465del XP_005269584.1:p.Phe155LeufsTer17
XM_011539282.1:c.465del XP_011537584.1:p.Phe155LeufsTer17
XR_945603.1:n.875del
XM_005269525.5:c.786del XP_005269582.1:p.Phe262LeufsTer17
XM_005269526.2:c.465del XP_005269583.1:p.Phe155LeufsTer17
XM_011539282.2:c.465del XP_011537584.1:p.Phe155LeufsTer17
XM_024447793.1:c.465del XP_024303561.1:p.Phe155LeufsTer17
XR_001747022.1:n.1064del
XR_001747023.1:n.958del
XR_945603.3:n.894del
NM_213649.2:c.813del MANE Select NP_998814.1:p.Phe271LeufsTer17