Canonical Allele Identifier: CA1939953730

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147863A= , CM000672.2:g.119147863A=	GRCh38
NC_000010.10:g.120907375A= , CM000672.1:g.120907375A=	GRCh37
NC_000010.9:g.120897365A=	NCBI36
NG_033895.1:g.22830T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.733-3T= MANE Select	ENSP00000347924.2:n.733-3T=
ENST00000355697.6:c.733-3T=	ENSP00000347924.2:n.733-3T=
ENST00000369131.8:c.385-3T=	ENSP00000358127.4:n.385-3T=
ENST00000461438.5:n.762-3T=
ENST00000466218.5:n.682-3T=
ENST00000484960.5:n.63-3T=
ENST00000490417.6:n.196-3T=
NM_213649.1:c.733-3T=	NP_998814.1:n.733-3T=
NR_110305.1:n.751-3T=
XM_005269525.3:c.706-3T=	XP_005269582.1:n.706-3T=
XM_005269526.1:c.385-3T=	XP_005269583.1:n.385-3T=
XM_005269527.1:c.385-3T=	XP_005269584.1:n.385-3T=
XM_011539282.1:c.385-3T=	XP_011537584.1:n.385-3T=
XR_945603.1:n.795-3T=
XM_005269525.5:c.706-3T=	XP_005269582.1:n.706-3T=
XM_005269526.2:c.385-3T=	XP_005269583.1:n.385-3T=
XM_011539282.2:c.385-3T=	XP_011537584.1:n.385-3T=
XM_024447793.1:c.385-3T=	XP_024303561.1:n.385-3T=
XR_001747022.1:n.984-3T=
XR_001747023.1:n.878-3T=
XR_945603.3:n.814-3T=
NM_213649.2:c.733-3T= MANE Select	NP_998814.1:n.733-3T=