Canonical Allele Identifier: CA5714388
Gene: SFXN4 HGNC NCBI

Linked Data

dbSNP Id: rs763755491

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119147778T>C , CM000672.2:g.119147778T>C GRCh38
NC_000010.10:g.120907290T>C , CM000672.1:g.120907290T>C GRCh37
NC_000010.9:g.120897280T>C NCBI36
NG_033895.1:g.22915A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355697.7:c.815A>G MANE Select ENSP00000347924.2:p.Lys272Arg
ENST00000355697.6:c.815A>G ENSP00000347924.2:p.Lys272Arg
ENST00000369131.8:c.467A>G ENSP00000358127.4:p.Lys156Arg
ENST00000461438.5:n.844A>G
ENST00000466218.5:n.764A>G
ENST00000484960.5:n.145A>G
ENST00000490417.6:n.278A>G
NM_213649.1:c.815A>G NP_998814.1:p.Lys272Arg
NR_110305.1:n.833A>G
XM_005269525.3:c.788A>G XP_005269582.1:p.Lys263Arg
XM_005269526.1:c.467A>G XP_005269583.1:p.Lys156Arg
XM_005269527.1:c.467A>G XP_005269584.1:p.Lys156Arg
XM_011539282.1:c.467A>G XP_011537584.1:p.Lys156Arg
XR_945603.1:n.877A>G
XM_005269525.5:c.788A>G XP_005269582.1:p.Lys263Arg
XM_005269526.2:c.467A>G XP_005269583.1:p.Lys156Arg
XM_011539282.2:c.467A>G XP_011537584.1:p.Lys156Arg
XM_024447793.1:c.467A>G XP_024303561.1:p.Lys156Arg
XR_001747022.1:n.1066A>G
XR_001747023.1:n.960A>G
XR_945603.3:n.896A>G
NM_213649.2:c.815A>G MANE Select NP_998814.1:p.Lys272Arg