Canonical Allele Identifier: CA7866620

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3600969G>A , CM000678.2:g.3600969G>A	GRCh38
NC_000016.9:g.3650970G>A , CM000678.1:g.3650970G>A	GRCh37
NC_000016.8:g.3590971G>A	NCBI36
NG_028123.1:g.15616C>T , LRG_503:g.15616C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697858.1:n.514C>T
ENST00000294008.4:c.1163+10C>T MANE Select	ENSP00000294008.3:n.1163+10C>T
ENST00000294008.3:c.1163+10C>T	ENSP00000294008.3:n.1163+10C>T
ENST00000466154.5:n.2384+10C>T
ENST00000486524.1:n.2727C>T
NM_032444.2:c.1163+10C>T , LRG_503t1:c.1163+10C>T	NP_115820.2:n.1163+10C>T
XM_011522715.1:c.1163+10C>T	XP_011521017.1:n.1163+10C>T
NM_032444.3:c.1163+10C>T	NP_115820.2:n.1163+10C>T
XM_011522715.3:c.1163+10C>T	XP_011521017.1:n.1163+10C>T
XM_017023775.2:c.-765+10C>T	XP_016879264.1:n.-765+10C>T
XM_024450471.1:c.1163+10C>T	XP_024306239.1:n.1163+10C>T
NM_032444.4:c.1163+10C>T MANE Select	NP_115820.2:n.1163+10C>T