Canonical Allele Identifier: CA394517166

Gene: SLX4

Linked Data

• MyVariant Identifiers: chr16:g.3639213T>A (hg19) ; chr16:g.3589212T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3589212T>A , CM000678.2:g.3589212T>A	GRCh38
NC_000016.9:g.3639213T>A , CM000678.1:g.3639213T>A	GRCh37
NC_000016.8:g.3579214T>A	NCBI36
NG_028123.1:g.27373A>T , LRG_503:g.27373A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.4426A>T MANE Select	ENSP00000294008.3:p.Thr1476Ser
ENST00000294008.3:c.4426A>T	ENSP00000294008.3:p.Thr1476Ser
NM_032444.2:c.4426A>T , LRG_503t1:c.4426A>T	NP_115820.2:p.Thr1476Ser
XM_011522715.1:c.4426A>T	XP_011521017.1:p.Thr1476Ser
NM_032444.3:c.4426A>T	NP_115820.2:p.Thr1476Ser
XM_011522715.3:c.4426A>T	XP_011521017.1:p.Thr1476Ser
XM_017023775.2:c.3604A>T	XP_016879264.1:p.Thr1202Ser
XM_024450471.1:c.4426A>T	XP_024306239.1:p.Thr1476Ser
NM_032444.4:c.4426A>T MANE Select	NP_115820.2:p.Thr1476Ser