Canonical Allele Identifier: CA1939953725

Gene: SFXN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147855A= , CM000672.2:g.119147855A=	GRCh38
NC_000010.10:g.120907367A= , CM000672.1:g.120907367A=	GRCh37
NC_000010.9:g.120897357A=	NCBI36
NG_033895.1:g.22838T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.738T= MANE Select	ENSP00000347924.2:p.Val246=
ENST00000355697.6:c.738T=	ENSP00000347924.2:p.Val246=
ENST00000369131.8:c.390T=	ENSP00000358127.4:p.Val130=
ENST00000461438.5:n.767T=
ENST00000466218.5:n.687T=
ENST00000484960.5:n.68T=
ENST00000490417.6:n.201T=
NM_213649.1:c.738T=	NP_998814.1:p.Val246=
NR_110305.1:n.756T=
XM_005269525.3:c.711T=	XP_005269582.1:p.Val237=
XM_005269526.1:c.390T=	XP_005269583.1:p.Val130=
XM_005269527.1:c.390T=	XP_005269584.1:p.Val130=
XM_011539282.1:c.390T=	XP_011537584.1:p.Val130=
XR_945603.1:n.800T=
XM_005269525.5:c.711T=	XP_005269582.1:p.Val237=
XM_005269526.2:c.390T=	XP_005269583.1:p.Val130=
XM_011539282.2:c.390T=	XP_011537584.1:p.Val130=
XM_024447793.1:c.390T=	XP_024303561.1:p.Val130=
XR_001747022.1:n.989T=
XR_001747023.1:n.883T=
XR_945603.3:n.819T=
NM_213649.2:c.738T= MANE Select	NP_998814.1:p.Val246=