Canonical Allele Identifier: CA53420436
Gene: SULT1C4 HGNC NCBI

Linked Data

dbSNP Id: rs1051707057

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378465C>A , CM000664.2:g.108378465C>A GRCh38
NC_000002.11:g.108994921C>A , CM000664.1:g.108994921C>A GRCh37
NC_000002.10:g.108361353C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.128C>A MANE Select ENSP00000272452.2:p.Ala43Asp
ENST00000272452.6:c.128C>A ENSP00000272452.2:p.Ala43Asp
ENST00000409309.3:c.128C>A ENSP00000387225.3:p.Ala43Asp
ENST00000494122.1:n.555C>A
NM_006588.2:c.128C>A NP_006579.2:p.Ala43Asp
XM_005263919.2:c.128C>A XP_005263976.1:p.Ala43Asp
NM_001321770.1:c.128C>A NP_001308699.1:p.Ala43Asp
NM_006588.3:c.128C>A NP_006579.2:p.Ala43Asp
NR_135776.1:n.555C>A
NR_135779.1:n.555C>A
XM_017003807.1:c.-193C>A XP_016859296.1:n.-193C>A
NM_006588.4:c.128C>A MANE Select NP_006579.2:p.Ala43Asp
NM_001321770.2:c.128C>A NP_001308699.1:p.Ala43Asp
NR_135776.2:n.512C>A
NR_135779.2:n.512C>A