Canonical Allele Identifier: CA2574686965

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147754G>C , CM000672.2:g.119147754G>C	GRCh38
NC_000010.10:g.120907266G>C , CM000672.1:g.120907266G>C	GRCh37
NC_000010.9:g.120897256G>C	NCBI36
NG_033895.1:g.22939C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.818+21C>G MANE Select	ENSP00000347924.2:n.818+21C>G
ENST00000355697.6:c.818+21C>G	ENSP00000347924.2:n.818+21C>G
ENST00000369131.8:c.470+21C>G	ENSP00000358127.4:n.470+21C>G
ENST00000461438.5:n.847+21C>G
ENST00000484960.5:n.148+21C>G
ENST00000490417.6:n.281+21C>G
NM_213649.1:c.818+21C>G	NP_998814.1:n.818+21C>G
NR_110305.1:n.836+21C>G
XM_005269525.3:c.791+21C>G	XP_005269582.1:n.791+21C>G
XM_005269526.1:c.470+21C>G	XP_005269583.1:n.470+21C>G
XM_005269527.1:c.470+21C>G	XP_005269584.1:n.470+21C>G
XM_011539282.1:c.470+21C>G	XP_011537584.1:n.470+21C>G
XR_945603.1:n.880+21C>G
XM_005269525.5:c.791+21C>G	XP_005269582.1:n.791+21C>G
XM_005269526.2:c.470+21C>G	XP_005269583.1:n.470+21C>G
XM_011539282.2:c.470+21C>G	XP_011537584.1:n.470+21C>G
XM_024447793.1:c.470+21C>G	XP_024303561.1:n.470+21C>G
XR_001747022.1:n.1069+21C>G
XR_001747023.1:n.963+21C>G
XR_945603.3:n.899+21C>G
NM_213649.2:c.818+21C>G MANE Select	NP_998814.1:n.818+21C>G