Canonical Allele Identifier: CA7865537

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3584768C>A , CM000678.2:g.3584768C>A	GRCh38
NC_000016.9:g.3634769C>A , CM000678.1:g.3634769C>A	GRCh37
NC_000016.8:g.3574770C>A	NCBI36
NG_028123.1:g.31817G>T , LRG_503:g.31817G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.4739+1G>T MANE Select	NP_115820.2:n.4739+1G>T
ENST00000294008.4:c.4739+1G>T MANE Select	ENSP00000294008.3:n.4739+1G>T
NM_032444.2:c.4739+1G>T , LRG_503t1:c.4739+1G>T	NP_115820.2:n.4739+1G>T
NM_032444.3:c.4739+1G>T	NP_115820.2:n.4739+1G>T
ENST00000294008.3:c.4739+1G>T	ENSP00000294008.3:n.4739+1G>T
XM_011522715.1:c.4736+1G>T	XP_011521017.1:n.4736+1G>T
XM_011522715.3:c.4736+1G>T	XP_011521017.1:n.4736+1G>T
XM_017023775.2:c.3917+1G>T	XP_016879264.1:n.3917+1G>T
XM_024450471.1:c.4739+1G>T	XP_024306239.1:n.4739+1G>T