Canonical Allele Identifier: CA2577062562
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378248_108378250del , CM000664.2:g.108378248_108378250del GRCh38
NC_000002.11:g.108994704_108994706del , CM000664.1:g.108994704_108994706del GRCh37
NC_000002.10:g.108361136_108361138del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-90_-88del MANE Select ENSP00000272452.2:n.-90_-88del
ENST00000272452.6:c.-90_-88del ENSP00000272452.2:n.-90_-88del
ENST00000409309.3:c.-90_-88del ENSP00000387225.3:n.-90_-88del
ENST00000494122.1:n.338_340del
NM_006588.2:c.-90_-88del NP_006579.2:n.-90_-88del
XM_005263919.2:c.-90_-88del XP_005263976.1:n.-90_-88del
NM_001321770.1:c.-90_-88del NP_001308699.1:n.-90_-88del
NM_006588.3:c.-90_-88del NP_006579.2:n.-90_-88del
NR_135776.1:n.338_340del
NR_135779.1:n.338_340del
NM_006588.4:c.-90_-88del MANE Select NP_006579.2:n.-90_-88del
NM_001321770.2:c.-90_-88del NP_001308699.1:n.-90_-88del
NR_135776.2:n.295_297del
NR_135779.2:n.295_297del