Canonical Allele Identifier: CA378271321

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907299T>G (hg19) ; chr10:g.119147787T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147787T>G , CM000672.2:g.119147787T>G	GRCh38
NC_000010.10:g.120907299T>G , CM000672.1:g.120907299T>G	GRCh37
NC_000010.9:g.120897289T>G	NCBI36
NG_033895.1:g.22906A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.806A>C MANE Select	ENSP00000347924.2:p.Tyr269Ser
ENST00000355697.6:c.806A>C	ENSP00000347924.2:p.Tyr269Ser
ENST00000369131.8:c.458A>C	ENSP00000358127.4:p.Tyr153Ser
ENST00000461438.5:n.835A>C
ENST00000466218.5:n.755A>C
ENST00000484960.5:n.136A>C
ENST00000490417.6:n.269A>C
NM_213649.1:c.806A>C	NP_998814.1:p.Tyr269Ser
NR_110305.1:n.824A>C
XM_005269525.3:c.779A>C	XP_005269582.1:p.Tyr260Ser
XM_005269526.1:c.458A>C	XP_005269583.1:p.Tyr153Ser
XM_005269527.1:c.458A>C	XP_005269584.1:p.Tyr153Ser
XM_011539282.1:c.458A>C	XP_011537584.1:p.Tyr153Ser
XR_945603.1:n.868A>C
XM_005269525.5:c.779A>C	XP_005269582.1:p.Tyr260Ser
XM_005269526.2:c.458A>C	XP_005269583.1:p.Tyr153Ser
XM_011539282.2:c.458A>C	XP_011537584.1:p.Tyr153Ser
XM_024447793.1:c.458A>C	XP_024303561.1:p.Tyr153Ser
XR_001747022.1:n.1057A>C
XR_001747023.1:n.951A>C
XR_945603.3:n.887A>C
NM_213649.2:c.806A>C MANE Select	NP_998814.1:p.Tyr269Ser