Canonical Allele Identifier: CA1939953607

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147548G= , CM000672.2:g.119147548G=	GRCh38
NC_000010.10:g.120907060G= , CM000672.1:g.120907060G=	GRCh37
NC_000010.9:g.120897050G=	NCBI36
NG_033895.1:g.23145C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.818+227C= MANE Select	ENSP00000347924.2:n.818+227C=
ENST00000355697.6:c.818+227C=	ENSP00000347924.2:n.818+227C=
ENST00000369131.8:c.470+227C=	ENSP00000358127.4:n.470+227C=
ENST00000461438.5:n.847+227C=
ENST00000484960.5:n.148+227C=
ENST00000490417.6:n.281+227C=
NM_213649.1:c.818+227C=	NP_998814.1:n.818+227C=
NR_110305.1:n.836+227C=
XM_005269525.3:c.791+227C=	XP_005269582.1:n.791+227C=
XM_005269526.1:c.470+227C=	XP_005269583.1:n.470+227C=
XM_005269527.1:c.470+227C=	XP_005269584.1:n.470+227C=
XM_011539282.1:c.470+227C=	XP_011537584.1:n.470+227C=
XR_945603.1:n.880+227C=
XM_005269525.5:c.791+227C=	XP_005269582.1:n.791+227C=
XM_005269526.2:c.470+227C=	XP_005269583.1:n.470+227C=
XM_011539282.2:c.470+227C=	XP_011537584.1:n.470+227C=
XM_024447793.1:c.470+227C=	XP_024303561.1:n.470+227C=
XR_001747022.1:n.1069+227C=
XR_001747023.1:n.963+227C=
XR_945603.3:n.899+227C=
NM_213649.2:c.818+227C= MANE Select	NP_998814.1:n.818+227C=