Canonical Allele Identifier: CA471625114

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907289T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147777T>C , CM000672.2:g.119147777T>C	GRCh38
NC_000010.10:g.120907289T>C , CM000672.1:g.120907289T>C	GRCh37
NC_000010.9:g.120897279T>C	NCBI36
NG_033895.1:g.22916A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.816A>G MANE Select	ENSP00000347924.2:p.Lys272=
ENST00000355697.6:c.816A>G	ENSP00000347924.2:p.Lys272=
ENST00000369131.8:c.468A>G	ENSP00000358127.4:p.Lys156=
ENST00000461438.5:n.845A>G
ENST00000484960.5:n.146A>G
ENST00000490417.6:n.279A>G
NM_213649.1:c.816A>G	NP_998814.1:p.Lys272=
NR_110305.1:n.834A>G
XM_005269525.3:c.789A>G	XP_005269582.1:p.Lys263=
XM_005269526.1:c.468A>G	XP_005269583.1:p.Lys156=
XM_005269527.1:c.468A>G	XP_005269584.1:p.Lys156=
XM_011539282.1:c.468A>G	XP_011537584.1:p.Lys156=
XR_945603.1:n.878A>G
XM_005269525.5:c.789A>G	XP_005269582.1:p.Lys263=
XM_005269526.2:c.468A>G	XP_005269583.1:p.Lys156=
XM_011539282.2:c.468A>G	XP_011537584.1:p.Lys156=
XM_024447793.1:c.468A>G	XP_024303561.1:p.Lys156=
XR_001747022.1:n.1067A>G
XR_001747023.1:n.961A>G
XR_945603.3:n.897A>G
NM_213649.2:c.816A>G MANE Select	NP_998814.1:p.Lys272=