Canonical Allele Identifier: CA378271293

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907294A>T (hg19) ; chr10:g.119147782A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147782A>T , CM000672.2:g.119147782A>T	GRCh38
NC_000010.10:g.120907294A>T , CM000672.1:g.120907294A>T	GRCh37
NC_000010.9:g.120897284A>T	NCBI36
NG_033895.1:g.22911T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.811T>A MANE Select	ENSP00000347924.2:p.Phe271Ile
ENST00000355697.6:c.811T>A	ENSP00000347924.2:p.Phe271Ile
ENST00000369131.8:c.463T>A	ENSP00000358127.4:p.Phe155Ile
ENST00000461438.5:n.840T>A
ENST00000466218.5:n.760T>A
ENST00000484960.5:n.141T>A
ENST00000490417.6:n.274T>A
NM_213649.1:c.811T>A	NP_998814.1:p.Phe271Ile
NR_110305.1:n.829T>A
XM_005269525.3:c.784T>A	XP_005269582.1:p.Phe262Ile
XM_005269526.1:c.463T>A	XP_005269583.1:p.Phe155Ile
XM_005269527.1:c.463T>A	XP_005269584.1:p.Phe155Ile
XM_011539282.1:c.463T>A	XP_011537584.1:p.Phe155Ile
XR_945603.1:n.873T>A
XM_005269525.5:c.784T>A	XP_005269582.1:p.Phe262Ile
XM_005269526.2:c.463T>A	XP_005269583.1:p.Phe155Ile
XM_011539282.2:c.463T>A	XP_011537584.1:p.Phe155Ile
XM_024447793.1:c.463T>A	XP_024303561.1:p.Phe155Ile
XR_001747022.1:n.1062T>A
XR_001747023.1:n.956T>A
XR_945603.3:n.892T>A
NM_213649.2:c.811T>A MANE Select	NP_998814.1:p.Phe271Ile