Canonical Allele Identifier: CA7865482

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3583377G>A , CM000678.2:g.3583377G>A	GRCh38
NC_000016.9:g.3633378G>A , CM000678.1:g.3633378G>A	GRCh37
NC_000016.8:g.3573379G>A	NCBI36
NG_028123.1:g.33208C>T , LRG_503:g.33208C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.4873C>T MANE Select	NP_115820.2:p.His1625Tyr
ENST00000294008.4:c.4873C>T MANE Select	ENSP00000294008.3:p.His1625Tyr
NM_032444.2:c.4873C>T , LRG_503t1:c.4873C>T	NP_115820.2:p.His1625Tyr
NM_032444.3:c.4873C>T	NP_115820.2:p.His1625Tyr
ENST00000294008.3:c.4873C>T	ENSP00000294008.3:p.His1625Tyr
XM_011522715.1:c.4870C>T	XP_011521017.1:p.His1624Tyr
XM_011522715.3:c.4870C>T	XP_011521017.1:p.His1624Tyr
XM_017023775.2:c.4051C>T	XP_016879264.1:p.His1351Tyr
XM_024450471.1:c.4873C>T	XP_024306239.1:p.His1625Tyr