Canonical Allele Identifier: CA378271261

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907288T>A (hg19) ; chr10:g.119147776T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147776T>A , CM000672.2:g.119147776T>A	GRCh38
NC_000010.10:g.120907288T>A , CM000672.1:g.120907288T>A	GRCh37
NC_000010.9:g.120897278T>A	NCBI36
NG_033895.1:g.22917A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.817A>T MANE Select	ENSP00000347924.2:p.Arg273Trp
ENST00000355697.6:c.817A>T	ENSP00000347924.2:p.Arg273Trp
ENST00000369131.8:c.469A>T	ENSP00000358127.4:p.Arg157Trp
ENST00000461438.5:n.846A>T
ENST00000484960.5:n.147A>T
ENST00000490417.6:n.280A>T
NM_213649.1:c.817A>T	NP_998814.1:p.Arg273Trp
NR_110305.1:n.835A>T
XM_005269525.3:c.790A>T	XP_005269582.1:p.Arg264Trp
XM_005269526.1:c.469A>T	XP_005269583.1:p.Arg157Trp
XM_005269527.1:c.469A>T	XP_005269584.1:p.Arg157Trp
XM_011539282.1:c.469A>T	XP_011537584.1:p.Arg157Trp
XR_945603.1:n.879A>T
XM_005269525.5:c.790A>T	XP_005269582.1:p.Arg264Trp
XM_005269526.2:c.469A>T	XP_005269583.1:p.Arg157Trp
XM_011539282.2:c.469A>T	XP_011537584.1:p.Arg157Trp
XM_024447793.1:c.469A>T	XP_024303561.1:p.Arg157Trp
XR_001747022.1:n.1068A>T
XR_001747023.1:n.962A>T
XR_945603.3:n.898A>T
NM_213649.2:c.817A>T MANE Select	NP_998814.1:p.Arg273Trp