Canonical Allele Identifier: CA378271312

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907298G>C (hg19) ; chr10:g.119147786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147786G>C , CM000672.2:g.119147786G>C	GRCh38
NC_000010.10:g.120907298G>C , CM000672.1:g.120907298G>C	GRCh37
NC_000010.9:g.120897288G>C	NCBI36
NG_033895.1:g.22907C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.807C>G MANE Select	ENSP00000347924.2:p.Tyr269Ter
ENST00000355697.6:c.807C>G	ENSP00000347924.2:p.Tyr269Ter
ENST00000369131.8:c.459C>G	ENSP00000358127.4:p.Tyr153Ter
ENST00000461438.5:n.836C>G
ENST00000466218.5:n.756C>G
ENST00000484960.5:n.137C>G
ENST00000490417.6:n.270C>G
NM_213649.1:c.807C>G	NP_998814.1:p.Tyr269Ter
NR_110305.1:n.825C>G
XM_005269525.3:c.780C>G	XP_005269582.1:p.Tyr260Ter
XM_005269526.1:c.459C>G	XP_005269583.1:p.Tyr153Ter
XM_005269527.1:c.459C>G	XP_005269584.1:p.Tyr153Ter
XM_011539282.1:c.459C>G	XP_011537584.1:p.Tyr153Ter
XR_945603.1:n.869C>G
XM_005269525.5:c.780C>G	XP_005269582.1:p.Tyr260Ter
XM_005269526.2:c.459C>G	XP_005269583.1:p.Tyr153Ter
XM_011539282.2:c.459C>G	XP_011537584.1:p.Tyr153Ter
XM_024447793.1:c.459C>G	XP_024303561.1:p.Tyr153Ter
XR_001747022.1:n.1058C>G
XR_001747023.1:n.952C>G
XR_945603.3:n.888C>G
NM_213649.2:c.807C>G MANE Select	NP_998814.1:p.Tyr269Ter