Canonical Allele Identifier: CA7865659

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3589249_3589259del , CM000678.2:g.3589249_3589259del	GRCh38
NC_000016.9:g.3639250_3639260del , CM000678.1:g.3639250_3639260del	GRCh37
NC_000016.8:g.3579251_3579261del	NCBI36
NG_028123.1:g.27328_27338del , LRG_503:g.27328_27338del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.4381_4391del MANE Select	ENSP00000294008.3:p.Ala1461ProfsTer2
ENST00000294008.3:c.4381_4391del	ENSP00000294008.3:p.Ala1461ProfsTer2
NM_032444.2:c.4381_4391del , LRG_503t1:c.4381_4391del	NP_115820.2:p.Ala1461ProfsTer2
XM_011522715.1:c.4381_4391del	XP_011521017.1:p.Ala1461ProfsTer2
NM_032444.3:c.4381_4391del	NP_115820.2:p.Ala1461ProfsTer2
XM_011522715.3:c.4381_4391del	XP_011521017.1:p.Ala1461ProfsTer2
XM_017023775.2:c.3559_3569del	XP_016879264.1:p.Ala1187ProfsTer2
XM_024450471.1:c.4381_4391del	XP_024306239.1:p.Ala1461ProfsTer2
NM_032444.4:c.4381_4391del MANE Select	NP_115820.2:p.Ala1461ProfsTer2