Canonical Allele Identifier: CA395442717

Gene: SLX1B SLX1B-SULT1A4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29457656C>T , CM000678.2:g.29457656C>T	GRCh38
NC_000016.9:g.29468977C>T , CM000678.1:g.29468977C>T	GRCh37
NC_000016.8:g.29376478C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024044.5:c.607C>T (SLX1B) MANE Select	NP_076949.1:p.Pro203Ser
ENST00000330181.10:c.607C>T (SLX1B) MANE Select	ENSP00000328940.5:p.Pro203Ser
NM_001400286.1:c.601C>T (SLX1B)	NP_001387215.1:p.Pro201Ser
NM_001400287.1:c.189-272C>T (SLX1B)	NP_001387216.1:n.189-272C>T
NM_024044.3:c.607C>T (SLX1B)	NP_076949.1:p.Pro203Ser
NM_024044.4:c.607C>T (SLX1B)	NP_076949.1:p.Pro203Ser
NM_178044.2:c.265C>T (SLX1B)	NP_835145.1:p.Pro89Ser
NM_178044.3:c.265C>T (SLX1B)	NP_835145.1:p.Pro89Ser
NM_178044.4:c.265C>T (SLX1B)	NP_835145.1:p.Pro89Ser
NR_037609.1:n.726C>T (SLX1B-SULT1A4)
ENST00000330181.9:c.607C>T (SLX1B)	ENSP00000328940.5:p.Pro203Ser
ENST00000351581.4:c.265C>T (SLX1B)	ENSP00000335316.4:p.Pro89Ser
ENST00000565219.1:n.1272C>T (SLX1B)
ENST00000566424.1:n.687C>T (SLX1B)