Canonical Allele Identifier: CA7865934

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3590274G>C , CM000678.2:g.3590274G>C	GRCh38
NC_000016.9:g.3640275G>C , CM000678.1:g.3640275G>C	GRCh37
NC_000016.8:g.3580276G>C	NCBI36
NG_028123.1:g.26311C>G , LRG_503:g.26311C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.3364C>G MANE Select	NP_115820.2:p.Pro1122Ala
ENST00000294008.4:c.3364C>G MANE Select	ENSP00000294008.3:p.Pro1122Ala
NM_032444.2:c.3364C>G , LRG_503t1:c.3364C>G	NP_115820.2:p.Pro1122Ala
NM_032444.3:c.3364C>G	NP_115820.2:p.Pro1122Ala
ENST00000294008.3:c.3364C>G	ENSP00000294008.3:p.Pro1122Ala
XM_011522715.1:c.3364C>G	XP_011521017.1:p.Pro1122Ala
XM_011522715.3:c.3364C>G	XP_011521017.1:p.Pro1122Ala
XM_017023775.2:c.2542C>G	XP_016879264.1:p.Pro848Ala
XM_024450471.1:c.3364C>G	XP_024306239.1:p.Pro1122Ala