Canonical Allele Identifier: CA2660578689
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378251A>G , CM000664.2:g.108378251A>G GRCh38
NC_000002.11:g.108994707A>G , CM000664.1:g.108994707A>G GRCh37
NC_000002.10:g.108361139A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-87A>G MANE Select ENSP00000272452.2:n.-87A>G
ENST00000272452.6:c.-87A>G ENSP00000272452.2:n.-87A>G
ENST00000409309.3:c.-87A>G ENSP00000387225.3:n.-87A>G
ENST00000494122.1:n.341A>G
NM_006588.2:c.-87A>G NP_006579.2:n.-87A>G
XM_005263919.2:c.-87A>G XP_005263976.1:n.-87A>G
NM_001321770.1:c.-87A>G NP_001308699.1:n.-87A>G
NM_006588.3:c.-87A>G NP_006579.2:n.-87A>G
NR_135776.1:n.341A>G
NR_135779.1:n.341A>G
NM_006588.4:c.-87A>G MANE Select NP_006579.2:n.-87A>G
NM_001321770.2:c.-87A>G NP_001308699.1:n.-87A>G
NR_135776.2:n.298A>G
NR_135779.2:n.298A>G