Canonical Allele Identifier: CA7866101

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3590957A>C , CM000678.2:g.3590957A>C	GRCh38
NC_000016.9:g.3640958A>C , CM000678.1:g.3640958A>C	GRCh37
NC_000016.8:g.3580959A>C	NCBI36
NG_028123.1:g.25628T>G , LRG_503:g.25628T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.2681T>G MANE Select	NP_115820.2:p.Val894Gly
ENST00000294008.4:c.2681T>G MANE Select	ENSP00000294008.3:p.Val894Gly
NM_032444.2:c.2681T>G , LRG_503t1:c.2681T>G	NP_115820.2:p.Val894Gly
NM_032444.3:c.2681T>G	NP_115820.2:p.Val894Gly
ENST00000294008.3:c.2681T>G	ENSP00000294008.3:p.Val894Gly
XM_011522715.1:c.2681T>G	XP_011521017.1:p.Val894Gly
XM_011522715.3:c.2681T>G	XP_011521017.1:p.Val894Gly
XM_017023775.2:c.1859T>G	XP_016879264.1:p.Val620Gly
XM_024450471.1:c.2681T>G	XP_024306239.1:p.Val894Gly