Canonical Allele Identifier: CA7866668

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3601192C>G , CM000678.2:g.3601192C>G	GRCh38
NC_000016.9:g.3651193C>G , CM000678.1:g.3651193C>G	GRCh37
NC_000016.8:g.3591194C>G	NCBI36
NG_028123.1:g.15393G>C , LRG_503:g.15393G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.951-1G>C MANE Select	NP_115820.2:n.951-1G>C
ENST00000294008.4:c.951-1G>C MANE Select	ENSP00000294008.3:n.951-1G>C
NM_032444.2:c.951-1G>C , LRG_503t1:c.951-1G>C	NP_115820.2:n.951-1G>C
NM_032444.3:c.951-1G>C	NP_115820.2:n.951-1G>C
ENST00000294008.3:c.951-1G>C	ENSP00000294008.3:n.951-1G>C
ENST00000466154.5:n.2171G>C
ENST00000486524.1:n.2504G>C
ENST00000697858.1:n.292-1G>C
XM_011522715.1:c.951-1G>C	XP_011521017.1:n.951-1G>C
XM_011522715.3:c.951-1G>C	XP_011521017.1:n.951-1G>C
XM_024450471.1:c.951-1G>C	XP_024306239.1:n.951-1G>C