Canonical Allele Identifier: CA7866273
Community Standard Title: NM_032444.4(SLX4):c.2160+8C>T
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3594445G>A , CM000678.2:g.3594445G>A GRCh38
NC_000016.9:g.3644446G>A , CM000678.1:g.3644446G>A GRCh37
NC_000016.8:g.3584447G>A NCBI36
NG_028123.1:g.22140C>T , LRG_503:g.22140C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.2160+8C>T MANE Select NP_115820.2:n.2160+8C>T
ENST00000294008.4:c.2160+8C>T MANE Select ENSP00000294008.3:n.2160+8C>T
NM_032444.2:c.2160+8C>T , LRG_503t1:c.2160+8C>T NP_115820.2:n.2160+8C>T
NM_032444.3:c.2160+8C>T NP_115820.2:n.2160+8C>T
ENST00000294008.3:c.2160+8C>T ENSP00000294008.3:n.2160+8C>T
XM_011522715.1:c.2160+8C>T XP_011521017.1:n.2160+8C>T
XM_011522715.3:c.2160+8C>T XP_011521017.1:n.2160+8C>T
XM_017023775.2:c.1338+8C>T XP_016879264.1:n.1338+8C>T
XM_024450471.1:c.2160+8C>T XP_024306239.1:n.2160+8C>T