Canonical Allele Identifier: CA2611135617

Gene: SFXN4

Linked Data

• gnomAD v4: 10-119147732-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147733dup , CM000672.2:g.119147733dup	GRCh38
NC_000010.10:g.120907245dup , CM000672.1:g.120907245dup	GRCh37
NC_000010.9:g.120897235dup	NCBI36
NG_033895.1:g.22960dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.818+42dup MANE Select	ENSP00000347924.2:n.818+42dup
ENST00000355697.6:c.818+42dup	ENSP00000347924.2:n.818+42dup
ENST00000369131.8:c.470+42dup	ENSP00000358127.4:n.470+42dup
ENST00000461438.5:n.847+42dup
ENST00000484960.5:n.148+42dup
ENST00000490417.6:n.281+42dup
NM_213649.1:c.818+42dup	NP_998814.1:n.818+42dup
NR_110305.1:n.836+42dup
XM_005269525.3:c.791+42dup	XP_005269582.1:n.791+42dup
XM_005269526.1:c.470+42dup	XP_005269583.1:n.470+42dup
XM_005269527.1:c.470+42dup	XP_005269584.1:n.470+42dup
XM_011539282.1:c.470+42dup	XP_011537584.1:n.470+42dup
XR_945603.1:n.880+42dup
XM_005269525.5:c.791+42dup	XP_005269582.1:n.791+42dup
XM_005269526.2:c.470+42dup	XP_005269583.1:n.470+42dup
XM_011539282.2:c.470+42dup	XP_011537584.1:n.470+42dup
XM_024447793.1:c.470+42dup	XP_024303561.1:n.470+42dup
XR_001747022.1:n.1069+42dup
XR_001747023.1:n.963+42dup
XR_945603.3:n.899+42dup
NM_213649.2:c.818+42dup MANE Select	NP_998814.1:n.818+42dup