Canonical Allele Identifier: CA394548087
Community Standard Title: NM_032444.4(SLX4):c.39C>G (p.Tyr13Ter)
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3608926G>C , CM000678.2:g.3608926G>C GRCh38
NC_000016.9:g.3658927G>C , CM000678.1:g.3658927G>C GRCh37
NC_000016.8:g.3598928G>C NCBI36
NG_028123.1:g.7659C>G , LRG_503:g.7659C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.39C>G MANE Select NP_115820.2:p.Tyr13Ter
ENST00000294008.4:c.39C>G MANE Select ENSP00000294008.3:p.Tyr13Ter
NM_032444.2:c.39C>G , LRG_503t1:c.39C>G NP_115820.2:p.Tyr13Ter
NM_032444.3:c.39C>G NP_115820.2:p.Tyr13Ter
ENST00000294008.3:c.39C>G ENSP00000294008.3:p.Tyr13Ter
ENST00000466154.5:n.334C>G
ENST00000486524.1:n.667C>G
ENST00000697859.1:n.661C>G
XM_011522715.1:c.39C>G XP_011521017.1:p.Tyr13Ter
XM_011522715.3:c.39C>G XP_011521017.1:p.Tyr13Ter
XM_024450471.1:c.39C>G XP_024306239.1:p.Tyr13Ter