Canonical Allele Identifier: CA348024389
Gene: SULT1C4 HGNC NCBI

Linked Data

dbSNP Id: rs1678303156

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378462A>T , CM000664.2:g.108378462A>T GRCh38
NC_000002.11:g.108994918A>T , CM000664.1:g.108994918A>T GRCh37
NC_000002.10:g.108361350A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.125A>T MANE Select ENSP00000272452.2:p.Gln42Leu
ENST00000272452.6:c.125A>T ENSP00000272452.2:p.Gln42Leu
ENST00000409309.3:c.125A>T ENSP00000387225.3:p.Gln42Leu
ENST00000494122.1:n.552A>T
NM_006588.2:c.125A>T NP_006579.2:p.Gln42Leu
XM_005263919.2:c.125A>T XP_005263976.1:p.Gln42Leu
NM_001321770.1:c.125A>T NP_001308699.1:p.Gln42Leu
NM_006588.3:c.125A>T NP_006579.2:p.Gln42Leu
NR_135776.1:n.552A>T
NR_135779.1:n.552A>T
XM_017003807.1:c.-196A>T XP_016859296.1:n.-196A>T
NM_006588.4:c.125A>T MANE Select NP_006579.2:p.Gln42Leu
NM_001321770.2:c.125A>T NP_001308699.1:p.Gln42Leu
NR_135776.2:n.509A>T
NR_135779.2:n.509A>T