Canonical Allele Identifier: CA1278105102

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1678295151

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378267_108378301dup , CM000664.2:g.108378267_108378301dup	GRCh38
NC_000002.11:g.108994723_108994757dup , CM000664.1:g.108994723_108994757dup	GRCh37
NC_000002.10:g.108361155_108361189dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.-71_-37dup MANE Select	ENSP00000272452.2:n.-71_-37dup
ENST00000272452.6:c.-71_-37dup	ENSP00000272452.2:n.-71_-37dup
ENST00000409309.3:c.-71_-37dup	ENSP00000387225.3:n.-71_-37dup
ENST00000494122.1:n.357_391dup
NM_006588.2:c.-71_-37dup	NP_006579.2:n.-71_-37dup
XM_005263919.2:c.-71_-37dup	XP_005263976.1:n.-71_-37dup
NM_001321770.1:c.-71_-37dup	NP_001308699.1:n.-71_-37dup
NM_006588.3:c.-71_-37dup	NP_006579.2:n.-71_-37dup
NR_135776.1:n.357_391dup
NR_135779.1:n.357_391dup
NM_006588.4:c.-71_-37dup MANE Select	NP_006579.2:n.-71_-37dup
NM_001321770.2:c.-71_-37dup	NP_001308699.1:n.-71_-37dup
NR_135776.2:n.314_348dup
NR_135779.2:n.314_348dup