Canonical Allele Identifier: CA534906234

Gene: SULT1C3

Linked Data

• dbSNP Id: rs1287393822
• gnomAD v2: 2-108875105-C-CTCCT
• gnomAD v3: 2-108258649-C-CTCCT
• gnomAD v4: 2-108258649-C-CTCCT
• MyVariant Identifiers: chr2:g.108875105_108875106insTCCT (hg19) ; chr2:g.108258649_108258650insTCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108258650_108258651insCCTT , CM000664.2:g.108258650_108258651insCCTT	GRCh38
NC_000002.11:g.108875106_108875107insCCTT , CM000664.1:g.108875106_108875107insCCTT	GRCh37
NC_000002.10:g.108241538_108241539insCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000681802.2:c.527-84_527-83insCCTT MANE Select	ENSP00000505748.1:n.527-84_527-83insCCTT
ENST00000329106.3:c.527-84_527-83insCCTT	ENSP00000333310.2:n.527-84_527-83insCCTT
ENST00000681802.1:c.527-84_527-83insCCTT	ENSP00000505748.1:n.527-84_527-83insCCTT
ENST00000329106.2:c.527-84_527-83insCCTT	ENSP00000333310.2:n.527-84_527-83insCCTT
NM_001008743.1:c.527-84_527-83insCCTT	NP_001008743.1:n.527-84_527-83insCCTT
XM_011511209.1:c.527-84_527-83insCCTT	XP_011509511.1:n.527-84_527-83insCCTT
XM_011511210.1:c.527-84_527-83insCCTT	XP_011509512.1:n.527-84_527-83insCCTT
XM_011511211.1:c.527-84_527-83insCCTT	XP_011509513.1:n.527-84_527-83insCCTT
XM_011511212.1:c.527-84_527-83insCCTT	XP_011509514.1:n.527-84_527-83insCCTT
NM_001008743.2:c.527-84_527-83insCCTT	NP_001008743.1:n.527-84_527-83insCCTT
NM_001320878.1:c.527-84_527-83insCCTT	NP_001307807.1:n.527-84_527-83insCCTT
XM_017004153.1:c.662-84_662-83insCCTT	XP_016859642.1:n.662-84_662-83insCCTT
XM_017004154.1:c.662-84_662-83insCCTT	XP_016859643.1:n.662-84_662-83insCCTT
XM_017004155.1:c.662-84_662-83insCCTT	XP_016859644.1:n.662-84_662-83insCCTT
NM_001008743.3:c.527-84_527-83insCCTT	NP_001008743.1:n.527-84_527-83insCCTT
NM_001320878.2:c.527-84_527-83insCCTT MANE Select	NP_001307807.1:n.527-84_527-83insCCTT