Canonical Allele Identifier: CA660629396

Gene: SFXN4

Linked Data

• dbSNP Id: rs1420073421
• gnomAD v3: 10-119147764-G-GT
• gnomAD v4: 10-119147764-G-GT
• MyVariant Identifiers: chr10:g.120907276_120907277insT (hg19) ; chr10:g.119147764_119147765insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147765dup , CM000672.2:g.119147765dup	GRCh38
NC_000010.10:g.120907277dup , CM000672.1:g.120907277dup	GRCh37
NC_000010.9:g.120897267dup	NCBI36
NG_033895.1:g.22928dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.818+10dup MANE Select	ENSP00000347924.2:n.818+10dup
ENST00000355697.6:c.818+10dup	ENSP00000347924.2:n.818+10dup
ENST00000369131.8:c.470+10dup	ENSP00000358127.4:n.470+10dup
ENST00000461438.5:n.847+10dup
ENST00000484960.5:n.148+10dup
ENST00000490417.6:n.281+10dup
NM_213649.1:c.818+10dup	NP_998814.1:n.818+10dup
NR_110305.1:n.836+10dup
XM_005269525.3:c.791+10dup	XP_005269582.1:n.791+10dup
XM_005269526.1:c.470+10dup	XP_005269583.1:n.470+10dup
XM_005269527.1:c.470+10dup	XP_005269584.1:n.470+10dup
XM_011539282.1:c.470+10dup	XP_011537584.1:n.470+10dup
XR_945603.1:n.880+10dup
XM_005269525.5:c.791+10dup	XP_005269582.1:n.791+10dup
XM_005269526.2:c.470+10dup	XP_005269583.1:n.470+10dup
XM_011539282.2:c.470+10dup	XP_011537584.1:n.470+10dup
XM_024447793.1:c.470+10dup	XP_024303561.1:n.470+10dup
XR_001747022.1:n.1069+10dup
XR_001747023.1:n.963+10dup
XR_945603.3:n.899+10dup
NM_213649.2:c.818+10dup MANE Select	NP_998814.1:n.818+10dup