Canonical Allele Identifier: CA471625175
Gene: SFXN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.120907367A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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