Canonical Allele Identifier: CA2660578709
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378283T>C , CM000664.2:g.108378283T>C GRCh38
NC_000002.11:g.108994739T>C , CM000664.1:g.108994739T>C GRCh37
NC_000002.10:g.108361171T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-55T>C MANE Select ENSP00000272452.2:n.-55T>C
ENST00000272452.6:c.-55T>C ENSP00000272452.2:n.-55T>C
ENST00000409309.3:c.-55T>C ENSP00000387225.3:n.-55T>C
ENST00000494122.1:n.373T>C
NM_006588.2:c.-55T>C NP_006579.2:n.-55T>C
XM_005263919.2:c.-55T>C XP_005263976.1:n.-55T>C
NM_001321770.1:c.-55T>C NP_001308699.1:n.-55T>C
NM_006588.3:c.-55T>C NP_006579.2:n.-55T>C
NR_135776.1:n.373T>C
NR_135779.1:n.373T>C
NM_006588.4:c.-55T>C MANE Select NP_006579.2:n.-55T>C
NM_001321770.2:c.-55T>C NP_001308699.1:n.-55T>C
NR_135776.2:n.330T>C
NR_135779.2:n.330T>C