Canonical Allele Identifier: CA2577062564
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378249G>A , CM000664.2:g.108378249G>A GRCh38
NC_000002.11:g.108994705G>A , CM000664.1:g.108994705G>A GRCh37
NC_000002.10:g.108361137G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-89G>A MANE Select ENSP00000272452.2:n.-89G>A
ENST00000272452.6:c.-89G>A ENSP00000272452.2:n.-89G>A
ENST00000409309.3:c.-89G>A ENSP00000387225.3:n.-89G>A
ENST00000494122.1:n.339G>A
NM_006588.2:c.-89G>A NP_006579.2:n.-89G>A
XM_005263919.2:c.-89G>A XP_005263976.1:n.-89G>A
NM_001321770.1:c.-89G>A NP_001308699.1:n.-89G>A
NM_006588.3:c.-89G>A NP_006579.2:n.-89G>A
NR_135776.1:n.339G>A
NR_135779.1:n.339G>A
NM_006588.4:c.-89G>A MANE Select NP_006579.2:n.-89G>A
NM_001321770.2:c.-89G>A NP_001308699.1:n.-89G>A
NR_135776.2:n.296G>A
NR_135779.2:n.296G>A