Canonical Allele Identifier: CA348024359
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378456A>C , CM000664.2:g.108378456A>C GRCh38
NC_000002.11:g.108994912A>C , CM000664.1:g.108994912A>C GRCh37
NC_000002.10:g.108361344A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.119A>C MANE Select ENSP00000272452.2:p.Asn40Thr
ENST00000272452.6:c.119A>C ENSP00000272452.2:p.Asn40Thr
ENST00000409309.3:c.119A>C ENSP00000387225.3:p.Asn40Thr
ENST00000494122.1:n.546A>C
NM_006588.2:c.119A>C NP_006579.2:p.Asn40Thr
XM_005263919.2:c.119A>C XP_005263976.1:p.Asn40Thr
NM_001321770.1:c.119A>C NP_001308699.1:p.Asn40Thr
NM_006588.3:c.119A>C NP_006579.2:p.Asn40Thr
NR_135776.1:n.546A>C
NR_135779.1:n.546A>C
XM_017003807.1:c.-202A>C XP_016859296.1:n.-202A>C
NM_006588.4:c.119A>C MANE Select NP_006579.2:p.Asn40Thr
NM_001321770.2:c.119A>C NP_001308699.1:p.Asn40Thr
NR_135776.2:n.503A>C
NR_135779.2:n.503A>C