Canonical Allele Identifier: CA2202844019

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3590269_3590273delinsAGACG , CM000678.2:g.3590269_3590273delinsAGACG	GRCh38
NC_000016.9:g.3640270_3640274delinsAGACG , CM000678.1:g.3640270_3640274delinsAGACG	GRCh37
NC_000016.8:g.3580271_3580275delinsAGACG	NCBI36
NG_028123.1:g.26312_26316delinsCGTCT , LRG_503:g.26312_26316delinsCGTCT

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.3365_3369delinsCGTCT MANE Select	NP_115820.2:p.Pro1122=
ENST00000294008.4:c.3365_3369delinsCGTCT MANE Select	ENSP00000294008.3:p.Pro1122=
NM_032444.2:c.3365_3369delinsCGTCT , LRG_503t1:c.3365_3369delinsCGTCT	NP_115820.2:p.Pro1122=
NM_032444.3:c.3365_3369delinsCGTCT	NP_115820.2:p.Pro1122=
ENST00000294008.3:c.3365_3369delinsCGTCT	ENSP00000294008.3:p.Pro1122=
XM_011522715.1:c.3365_3369delinsCGTCT	XP_011521017.1:p.Pro1122=
XM_011522715.3:c.3365_3369delinsCGTCT	XP_011521017.1:p.Pro1122=
XM_017023775.2:c.2543_2547delinsCGTCT	XP_016879264.1:p.Pro848=
XM_024450471.1:c.3365_3369delinsCGTCT	XP_024306239.1:p.Pro1122=