Canonical Allele Identifier: CA2611135633

Gene: SFXN4

Linked Data

• gnomAD v4: 10-119147870-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147870A>G , CM000672.2:g.119147870A>G	GRCh38
NC_000010.10:g.120907382A>G , CM000672.1:g.120907382A>G	GRCh37
NC_000010.9:g.120897372A>G	NCBI36
NG_033895.1:g.22823T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355697.7:c.733-10T>C MANE Select	ENSP00000347924.2:n.733-10T>C
ENST00000355697.6:c.733-10T>C	ENSP00000347924.2:n.733-10T>C
ENST00000369131.8:c.385-10T>C	ENSP00000358127.4:n.385-10T>C
ENST00000461438.5:n.762-10T>C
ENST00000466218.5:n.682-10T>C
ENST00000484960.5:n.63-10T>C
ENST00000490417.6:n.196-10T>C
NM_213649.1:c.733-10T>C	NP_998814.1:n.733-10T>C
NR_110305.1:n.751-10T>C
XM_005269525.3:c.706-10T>C	XP_005269582.1:n.706-10T>C
XM_005269526.1:c.385-10T>C	XP_005269583.1:n.385-10T>C
XM_005269527.1:c.385-10T>C	XP_005269584.1:n.385-10T>C
XM_011539282.1:c.385-10T>C	XP_011537584.1:n.385-10T>C
XR_945603.1:n.795-10T>C
XM_005269525.5:c.706-10T>C	XP_005269582.1:n.706-10T>C
XM_005269526.2:c.385-10T>C	XP_005269583.1:n.385-10T>C
XM_011539282.2:c.385-10T>C	XP_011537584.1:n.385-10T>C
XM_024447793.1:c.385-10T>C	XP_024303561.1:n.385-10T>C
XR_001747022.1:n.984-10T>C
XR_001747023.1:n.878-10T>C
XR_945603.3:n.814-10T>C
NM_213649.2:c.733-10T>C MANE Select	NP_998814.1:n.733-10T>C