Canonical Allele Identifier: CA7865565

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3584888A>C , CM000678.2:g.3584888A>C	GRCh38
NC_000016.9:g.3634889A>C , CM000678.1:g.3634889A>C	GRCh37
NC_000016.8:g.3574890A>C	NCBI36
NG_028123.1:g.31697T>G , LRG_503:g.31697T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.4637-17T>G MANE Select	NP_115820.2:n.4637-17T>G
ENST00000294008.4:c.4637-17T>G MANE Select	ENSP00000294008.3:n.4637-17T>G
NM_032444.2:c.4637-17T>G , LRG_503t1:c.4637-17T>G	NP_115820.2:n.4637-17T>G
NM_032444.3:c.4637-17T>G	NP_115820.2:n.4637-17T>G
ENST00000294008.3:c.4637-17T>G	ENSP00000294008.3:n.4637-17T>G
XM_011522715.1:c.4637-20T>G	XP_011521017.1:n.4637-20T>G
XM_011522715.3:c.4637-20T>G	XP_011521017.1:n.4637-20T>G
XM_017023775.2:c.3815-17T>G	XP_016879264.1:n.3815-17T>G
XM_024450471.1:c.4637-17T>G	XP_024306239.1:n.4637-17T>G