Canonical Allele Identifier: CA378271631

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907373C>A (hg19) ; chr10:g.119147861C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147861C>A , CM000672.2:g.119147861C>A	GRCh38
NC_000010.10:g.120907373C>A , CM000672.1:g.120907373C>A	GRCh37
NC_000010.9:g.120897363C>A	NCBI36
NG_033895.1:g.22832G>T

Transcript Alleles

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