Canonical Allele Identifier: CA394515273
Community Standard Title: NM_032444.4(SLX4):c.4837G>T (p.Glu1613Ter)
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3583413C>A , CM000678.2:g.3583413C>A GRCh38
NC_000016.9:g.3633414C>A , CM000678.1:g.3633414C>A GRCh37
NC_000016.8:g.3573415C>A NCBI36
NG_028123.1:g.33172G>T , LRG_503:g.33172G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.4837G>T MANE Select NP_115820.2:p.Glu1613Ter
ENST00000294008.4:c.4837G>T MANE Select ENSP00000294008.3:p.Glu1613Ter
NM_032444.2:c.4837G>T , LRG_503t1:c.4837G>T NP_115820.2:p.Glu1613Ter
NM_032444.3:c.4837G>T NP_115820.2:p.Glu1613Ter
ENST00000294008.3:c.4837G>T ENSP00000294008.3:p.Glu1613Ter
XM_011522715.1:c.4834G>T XP_011521017.1:p.Glu1612Ter
XM_011522715.3:c.4834G>T XP_011521017.1:p.Glu1612Ter
XM_017023775.2:c.4015G>T XP_016879264.1:p.Glu1339Ter
XM_024450471.1:c.4837G>T XP_024306239.1:p.Glu1613Ter