Canonical Allele Identifier: CA1939953696

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147790G= , CM000672.2:g.119147790G=	GRCh38
NC_000010.10:g.120907302G= , CM000672.1:g.120907302G=	GRCh37
NC_000010.9:g.120897292G=	NCBI36
NG_033895.1:g.22903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.803C= MANE Select	ENSP00000347924.2:p.Thr268=
ENST00000355697.6:c.803C=	ENSP00000347924.2:p.Thr268=
ENST00000369131.8:c.455C=	ENSP00000358127.4:p.Thr152=
ENST00000461438.5:n.832C=
ENST00000466218.5:n.752C=
ENST00000484960.5:n.133C=
ENST00000490417.6:n.266C=
NM_213649.1:c.803C=	NP_998814.1:p.Thr268=
NR_110305.1:n.821C=
XM_005269525.3:c.776C=	XP_005269582.1:p.Thr259=
XM_005269526.1:c.455C=	XP_005269583.1:p.Thr152=
XM_005269527.1:c.455C=	XP_005269584.1:p.Thr152=
XM_011539282.1:c.455C=	XP_011537584.1:p.Thr152=
XR_945603.1:n.865C=
XM_005269525.5:c.776C=	XP_005269582.1:p.Thr259=
XM_005269526.2:c.455C=	XP_005269583.1:p.Thr152=
XM_011539282.2:c.455C=	XP_011537584.1:p.Thr152=
XM_024447793.1:c.455C=	XP_024303561.1:p.Thr152=
XR_001747022.1:n.1054C=
XR_001747023.1:n.948C=
XR_945603.3:n.884C=
NM_213649.2:c.803C= MANE Select	NP_998814.1:p.Thr268=