Canonical Allele Identifier: CA2660580178
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108387226C>A , CM000664.2:g.108387226C>A GRCh38
NC_000002.11:g.109003682C>A , CM000664.1:g.109003682C>A GRCh37
NC_000002.10:g.108370114C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.797-94C>A MANE Select ENSP00000272452.2:n.797-94C>A
ENST00000272452.6:c.797-94C>A ENSP00000272452.2:n.797-94C>A
ENST00000409309.3:c.572-94C>A ENSP00000387225.3:n.572-94C>A
NM_006588.2:c.797-94C>A NP_006579.2:n.797-94C>A
XM_005263919.2:c.572-94C>A XP_005263976.1:n.572-94C>A
NM_001321770.1:c.572-94C>A NP_001308699.1:n.572-94C>A
NM_006588.3:c.797-94C>A NP_006579.2:n.797-94C>A
NR_135776.1:n.1049-94C>A
NR_135779.1:n.778-94C>A
XM_017003807.1:c.527-94C>A XP_016859296.1:n.527-94C>A
NM_006588.4:c.797-94C>A MANE Select NP_006579.2:n.797-94C>A
NM_001321770.2:c.572-94C>A NP_001308699.1:n.572-94C>A
NR_135776.2:n.1006-94C>A
NR_135779.2:n.735-94C>A