Canonical Allele Identifier: CA1939953728
Gene: SFXN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119147861C= , CM000672.2:g.119147861C= GRCh38
NC_000010.10:g.120907373C= , CM000672.1:g.120907373C= GRCh37
NC_000010.9:g.120897363C= NCBI36
NG_033895.1:g.22832G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355697.7:c.733-1G= MANE Select ENSP00000347924.2:n.733-1G=
ENST00000355697.6:c.733-1G= ENSP00000347924.2:n.733-1G=
ENST00000369131.8:c.385-1G= ENSP00000358127.4:n.385-1G=
ENST00000461438.5:n.762-1G=
ENST00000466218.5:n.682-1G=
ENST00000484960.5:n.63-1G=
ENST00000490417.6:n.196-1G=
NM_213649.1:c.733-1G= NP_998814.1:n.733-1G=
NR_110305.1:n.751-1G=
XM_005269525.3:c.706-1G= XP_005269582.1:n.706-1G=
XM_005269526.1:c.385-1G= XP_005269583.1:n.385-1G=
XM_005269527.1:c.385-1G= XP_005269584.1:n.385-1G=
XM_011539282.1:c.385-1G= XP_011537584.1:n.385-1G=
XR_945603.1:n.795-1G=
XM_005269525.5:c.706-1G= XP_005269582.1:n.706-1G=
XM_005269526.2:c.385-1G= XP_005269583.1:n.385-1G=
XM_011539282.2:c.385-1G= XP_011537584.1:n.385-1G=
XM_024447793.1:c.385-1G= XP_024303561.1:n.385-1G=
XR_001747022.1:n.984-1G=
XR_001747023.1:n.878-1G=
XR_945603.3:n.814-1G=
NM_213649.2:c.733-1G= MANE Select NP_998814.1:n.733-1G=