Canonical Allele Identifier: CA394525240
Community Standard Title: NM_032444.4(SLX4):c.2161-2A>T
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3592867T>A , CM000678.2:g.3592867T>A GRCh38
NC_000016.9:g.3642868T>A , CM000678.1:g.3642868T>A GRCh37
NC_000016.8:g.3582869T>A NCBI36
NG_028123.1:g.23718A>T , LRG_503:g.23718A>T

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.2161-2A>T MANE Select NP_115820.2:n.2161-2A>T
ENST00000294008.4:c.2161-2A>T MANE Select ENSP00000294008.3:n.2161-2A>T
NM_032444.2:c.2161-2A>T , LRG_503t1:c.2161-2A>T NP_115820.2:n.2161-2A>T
NM_032444.3:c.2161-2A>T NP_115820.2:n.2161-2A>T
ENST00000294008.3:c.2161-2A>T ENSP00000294008.3:n.2161-2A>T
XM_011522715.1:c.2161-2A>T XP_011521017.1:n.2161-2A>T
XM_011522715.3:c.2161-2A>T XP_011521017.1:n.2161-2A>T
XM_017023775.2:c.1339-2A>T XP_016879264.1:n.1339-2A>T
XM_024450471.1:c.2161-2A>T XP_024306239.1:n.2161-2A>T