Canonical Allele Identifier: CA394516823

Gene: SLX4

Linked Data

• MyVariant Identifiers: chr16:g.3639049C>G (hg19) ; chr16:g.3589048C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3589048C>G , CM000678.2:g.3589048C>G	GRCh38
NC_000016.9:g.3639049C>G , CM000678.1:g.3639049C>G	GRCh37
NC_000016.8:g.3579050C>G	NCBI36
NG_028123.1:g.27537G>C , LRG_503:g.27537G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.4590G>C MANE Select	ENSP00000294008.3:p.Met1530Ile
ENST00000294008.3:c.4590G>C	ENSP00000294008.3:p.Met1530Ile
NM_032444.2:c.4590G>C , LRG_503t1:c.4590G>C	NP_115820.2:p.Met1530Ile
XM_011522715.1:c.4590G>C	XP_011521017.1:p.Met1530Ile
NM_032444.3:c.4590G>C	NP_115820.2:p.Met1530Ile
XM_011522715.3:c.4590G>C	XP_011521017.1:p.Met1530Ile
XM_017023775.2:c.3768G>C	XP_016879264.1:p.Met1256Ile
XM_024450471.1:c.4590G>C	XP_024306239.1:p.Met1530Ile
NM_032444.4:c.4590G>C MANE Select	NP_115820.2:p.Met1530Ile