Canonical Allele Identifier: CA2789688669

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147871_119147872del , CM000672.2:g.119147871_119147872del	GRCh38
NC_000010.10:g.120907383_120907384del , CM000672.1:g.120907383_120907384del	GRCh37
NC_000010.9:g.120897373_120897374del	NCBI36
NG_033895.1:g.22821_22822del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.733-12_733-11del MANE Select	ENSP00000347924.2:n.733-12_733-11del
ENST00000355697.6:c.733-12_733-11del	ENSP00000347924.2:n.733-12_733-11del
ENST00000369131.8:c.385-12_385-11del	ENSP00000358127.4:n.385-12_385-11del
ENST00000461438.5:n.762-12_762-11del
ENST00000466218.5:n.682-12_682-11del
ENST00000484960.5:n.63-12_63-11del
ENST00000490417.6:n.196-12_196-11del
NM_213649.1:c.733-12_733-11del	NP_998814.1:n.733-12_733-11del
NR_110305.1:n.751-12_751-11del
XM_005269525.3:c.706-12_706-11del	XP_005269582.1:n.706-12_706-11del
XM_005269526.1:c.385-12_385-11del	XP_005269583.1:n.385-12_385-11del
XM_005269527.1:c.385-12_385-11del	XP_005269584.1:n.385-12_385-11del
XM_011539282.1:c.385-12_385-11del	XP_011537584.1:n.385-12_385-11del
XR_945603.1:n.795-12_795-11del
XM_005269525.5:c.706-12_706-11del	XP_005269582.1:n.706-12_706-11del
XM_005269526.2:c.385-12_385-11del	XP_005269583.1:n.385-12_385-11del
XM_011539282.2:c.385-12_385-11del	XP_011537584.1:n.385-12_385-11del
XM_024447793.1:c.385-12_385-11del	XP_024303561.1:n.385-12_385-11del
XR_001747022.1:n.984-12_984-11del
XR_001747023.1:n.878-12_878-11del
XR_945603.3:n.814-12_814-11del
NM_213649.2:c.733-12_733-11del MANE Select	NP_998814.1:n.733-12_733-11del