Canonical Allele Identifier: CA7865918

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3590181G>C , CM000678.2:g.3590181G>C	GRCh38
NC_000016.9:g.3640182G>C , CM000678.1:g.3640182G>C	GRCh37
NC_000016.8:g.3580183G>C	NCBI36
NG_028123.1:g.26404C>G , LRG_503:g.26404C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.3457C>G MANE Select	NP_115820.2:p.Leu1153Val
ENST00000294008.4:c.3457C>G MANE Select	ENSP00000294008.3:p.Leu1153Val
NM_032444.2:c.3457C>G , LRG_503t1:c.3457C>G	NP_115820.2:p.Leu1153Val
NM_032444.3:c.3457C>G	NP_115820.2:p.Leu1153Val
ENST00000294008.3:c.3457C>G	ENSP00000294008.3:p.Leu1153Val
XM_011522715.1:c.3457C>G	XP_011521017.1:p.Leu1153Val
XM_011522715.3:c.3457C>G	XP_011521017.1:p.Leu1153Val
XM_017023775.2:c.2635C>G	XP_016879264.1:p.Leu879Val
XM_024450471.1:c.3457C>G	XP_024306239.1:p.Leu1153Val