Canonical Allele Identifier: CA534691749

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1435607009
• gnomAD v2: 2-108994799-CT-C
• MyVariant Identifiers: chr2:g.108994800del (hg19) ; chr2:g.108378344del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378345del , CM000664.2:g.108378345del	GRCh38
NC_000002.11:g.108994801del , CM000664.1:g.108994801del	GRCh37
NC_000002.10:g.108361233del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.8del MANE Select	ENSP00000272452.2:p.Leu3TyrfsTer15
ENST00000272452.6:c.8del	ENSP00000272452.2:p.Leu3TyrfsTer15
ENST00000409309.3:c.8del	ENSP00000387225.3:p.Leu3TyrfsTer15
ENST00000494122.1:n.435del
NM_006588.2:c.8del	NP_006579.2:p.Leu3TyrfsTer15
XM_005263919.2:c.8del	XP_005263976.1:p.Leu3TyrfsTer15
NM_001321770.1:c.8del	NP_001308699.1:p.Leu3TyrfsTer15
NM_006588.3:c.8del	NP_006579.2:p.Leu3TyrfsTer15
NR_135776.1:n.435del
NR_135779.1:n.435del
NM_006588.4:c.8del MANE Select	NP_006579.2:p.Leu3TyrfsTer15
NM_001321770.2:c.8del	NP_001308699.1:p.Leu3TyrfsTer15
NR_135776.2:n.392del
NR_135779.2:n.392del