Canonical Allele Identifier: CA394526092

Gene: SLX4

Linked Data

• dbSNP Id: rs73505420
• MyVariant Identifiers: chr16:g.3644511C>A (hg19) ; chr16:g.3594510C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3594510C>A , CM000678.2:g.3594510C>A	GRCh38
NC_000016.9:g.3644511C>A , CM000678.1:g.3644511C>A	GRCh37
NC_000016.8:g.3584512C>A	NCBI36
NG_028123.1:g.22075G>T , LRG_503:g.22075G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.2103G>T MANE Select	ENSP00000294008.3:p.Glu701Asp
ENST00000294008.3:c.2103G>T	ENSP00000294008.3:p.Glu701Asp
NM_032444.2:c.2103G>T , LRG_503t1:c.2103G>T	NP_115820.2:p.Glu701Asp
XM_011522715.1:c.2103G>T	XP_011521017.1:p.Glu701Asp
NM_032444.3:c.2103G>T	NP_115820.2:p.Glu701Asp
XM_011522715.3:c.2103G>T	XP_011521017.1:p.Glu701Asp
XM_017023775.2:c.1281G>T	XP_016879264.1:p.Glu427Asp
XM_024450471.1:c.2103G>T	XP_024306239.1:p.Glu701Asp
NM_032444.4:c.2103G>T MANE Select	NP_115820.2:p.Glu701Asp