Canonical Allele Identifier: CA378271334

Gene: SFXN4

Linked Data

• gnomAD v4: 10-119147790-G-C
• MyVariant Identifiers: chr10:g.120907302G>C (hg19) ; chr10:g.119147790G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147790G>C , CM000672.2:g.119147790G>C	GRCh38
NC_000010.10:g.120907302G>C , CM000672.1:g.120907302G>C	GRCh37
NC_000010.9:g.120897292G>C	NCBI36
NG_033895.1:g.22903C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.803C>G MANE Select	ENSP00000347924.2:p.Thr268Ser
ENST00000355697.6:c.803C>G	ENSP00000347924.2:p.Thr268Ser
ENST00000369131.8:c.455C>G	ENSP00000358127.4:p.Thr152Ser
ENST00000461438.5:n.832C>G
ENST00000466218.5:n.752C>G
ENST00000484960.5:n.133C>G
ENST00000490417.6:n.266C>G
NM_213649.1:c.803C>G	NP_998814.1:p.Thr268Ser
NR_110305.1:n.821C>G
XM_005269525.3:c.776C>G	XP_005269582.1:p.Thr259Ser
XM_005269526.1:c.455C>G	XP_005269583.1:p.Thr152Ser
XM_005269527.1:c.455C>G	XP_005269584.1:p.Thr152Ser
XM_011539282.1:c.455C>G	XP_011537584.1:p.Thr152Ser
XR_945603.1:n.865C>G
XM_005269525.5:c.776C>G	XP_005269582.1:p.Thr259Ser
XM_005269526.2:c.455C>G	XP_005269583.1:p.Thr152Ser
XM_011539282.2:c.455C>G	XP_011537584.1:p.Thr152Ser
XM_024447793.1:c.455C>G	XP_024303561.1:p.Thr152Ser
XR_001747022.1:n.1054C>G
XR_001747023.1:n.948C>G
XR_945603.3:n.884C>G
NM_213649.2:c.803C>G MANE Select	NP_998814.1:p.Thr268Ser