Canonical Allele Identifier: CA7865877

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3589976G>A , CM000678.2:g.3589976G>A	GRCh38
NC_000016.9:g.3639977G>A , CM000678.1:g.3639977G>A	GRCh37
NC_000016.8:g.3579978G>A	NCBI36
NG_028123.1:g.26609C>T , LRG_503:g.26609C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.3662C>T MANE Select	ENSP00000294008.3:p.Ala1221Val
ENST00000294008.3:c.3662C>T	ENSP00000294008.3:p.Ala1221Val
NM_032444.2:c.3662C>T , LRG_503t1:c.3662C>T	NP_115820.2:p.Ala1221Val
XM_011522715.1:c.3662C>T	XP_011521017.1:p.Ala1221Val
NM_032444.3:c.3662C>T	NP_115820.2:p.Ala1221Val
XM_011522715.3:c.3662C>T	XP_011521017.1:p.Ala1221Val
XM_017023775.2:c.2840C>T	XP_016879264.1:p.Ala947Val
XM_024450471.1:c.3662C>T	XP_024306239.1:p.Ala1221Val
NM_032444.4:c.3662C>T MANE Select	NP_115820.2:p.Ala1221Val