Canonical Allele Identifier: CA1939953693

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147778T= , CM000672.2:g.119147778T=	GRCh38
NC_000010.10:g.120907290T= , CM000672.1:g.120907290T=	GRCh37
NC_000010.9:g.120897280T=	NCBI36
NG_033895.1:g.22915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.815A= MANE Select	ENSP00000347924.2:p.Lys272=
ENST00000355697.6:c.815A=	ENSP00000347924.2:p.Lys272=
ENST00000369131.8:c.467A=	ENSP00000358127.4:p.Lys156=
ENST00000461438.5:n.844A=
ENST00000466218.5:n.764A=
ENST00000484960.5:n.145A=
ENST00000490417.6:n.278A=
NM_213649.1:c.815A=	NP_998814.1:p.Lys272=
NR_110305.1:n.833A=
XM_005269525.3:c.788A=	XP_005269582.1:p.Lys263=
XM_005269526.1:c.467A=	XP_005269583.1:p.Lys156=
XM_005269527.1:c.467A=	XP_005269584.1:p.Lys156=
XM_011539282.1:c.467A=	XP_011537584.1:p.Lys156=
XR_945603.1:n.877A=
XM_005269525.5:c.788A=	XP_005269582.1:p.Lys263=
XM_005269526.2:c.467A=	XP_005269583.1:p.Lys156=
XM_011539282.2:c.467A=	XP_011537584.1:p.Lys156=
XM_024447793.1:c.467A=	XP_024303561.1:p.Lys156=
XR_001747022.1:n.1066A=
XR_001747023.1:n.960A=
XR_945603.3:n.896A=
NM_213649.2:c.815A= MANE Select	NP_998814.1:p.Lys272=