Canonical Allele Identifier: CA2789688672

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147876_119147877insAC , CM000672.2:g.119147876_119147877insAC	GRCh38
NC_000010.10:g.120907388_120907389insAC , CM000672.1:g.120907388_120907389insAC	GRCh37
NC_000010.9:g.120897378_120897379insAC	NCBI36
NG_033895.1:g.22816_22817insGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.733-17_733-16insGT MANE Select	ENSP00000347924.2:n.733-17_733-16insGT
ENST00000355697.6:c.733-17_733-16insGT	ENSP00000347924.2:n.733-17_733-16insGT
ENST00000369131.8:c.385-17_385-16insGT	ENSP00000358127.4:n.385-17_385-16insGT
ENST00000461438.5:n.762-17_762-16insGT
ENST00000466218.5:n.682-17_682-16insGT
ENST00000484960.5:n.63-17_63-16insGT
ENST00000490417.6:n.196-17_196-16insGT
NM_213649.1:c.733-17_733-16insGT	NP_998814.1:n.733-17_733-16insGT
NR_110305.1:n.751-17_751-16insGT
XM_005269525.3:c.706-17_706-16insGT	XP_005269582.1:n.706-17_706-16insGT
XM_005269526.1:c.385-17_385-16insGT	XP_005269583.1:n.385-17_385-16insGT
XM_005269527.1:c.385-17_385-16insGT	XP_005269584.1:n.385-17_385-16insGT
XM_011539282.1:c.385-17_385-16insGT	XP_011537584.1:n.385-17_385-16insGT
XR_945603.1:n.795-17_795-16insGT
XM_005269525.5:c.706-17_706-16insGT	XP_005269582.1:n.706-17_706-16insGT
XM_005269526.2:c.385-17_385-16insGT	XP_005269583.1:n.385-17_385-16insGT
XM_011539282.2:c.385-17_385-16insGT	XP_011537584.1:n.385-17_385-16insGT
XM_024447793.1:c.385-17_385-16insGT	XP_024303561.1:n.385-17_385-16insGT
XR_001747022.1:n.984-17_984-16insGT
XR_001747023.1:n.878-17_878-16insGT
XR_945603.3:n.814-17_814-16insGT
NM_213649.2:c.733-17_733-16insGT MANE Select	NP_998814.1:n.733-17_733-16insGT