Canonical Allele Identifier: CA378271328

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907300A>G (hg19) ; chr10:g.119147788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147788A>G , CM000672.2:g.119147788A>G	GRCh38
NC_000010.10:g.120907300A>G , CM000672.1:g.120907300A>G	GRCh37
NC_000010.9:g.120897290A>G	NCBI36
NG_033895.1:g.22905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.805T>C MANE Select	ENSP00000347924.2:p.Tyr269His
ENST00000355697.6:c.805T>C	ENSP00000347924.2:p.Tyr269His
ENST00000369131.8:c.457T>C	ENSP00000358127.4:p.Tyr153His
ENST00000461438.5:n.834T>C
ENST00000466218.5:n.754T>C
ENST00000484960.5:n.135T>C
ENST00000490417.6:n.268T>C
NM_213649.1:c.805T>C	NP_998814.1:p.Tyr269His
NR_110305.1:n.823T>C
XM_005269525.3:c.778T>C	XP_005269582.1:p.Tyr260His
XM_005269526.1:c.457T>C	XP_005269583.1:p.Tyr153His
XM_005269527.1:c.457T>C	XP_005269584.1:p.Tyr153His
XM_011539282.1:c.457T>C	XP_011537584.1:p.Tyr153His
XR_945603.1:n.867T>C
XM_005269525.5:c.778T>C	XP_005269582.1:p.Tyr260His
XM_005269526.2:c.457T>C	XP_005269583.1:p.Tyr153His
XM_011539282.2:c.457T>C	XP_011537584.1:p.Tyr153His
XM_024447793.1:c.457T>C	XP_024303561.1:p.Tyr153His
XR_001747022.1:n.1056T>C
XR_001747023.1:n.950T>C
XR_945603.3:n.886T>C
NM_213649.2:c.805T>C MANE Select	NP_998814.1:p.Tyr269His