Canonical Allele Identifier: CA646969271
Gene: SULT1C4 HGNC NCBI

Linked Data

gnomAD v4: 2-108378247-G-A
COSMIC: COSN8922836
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378247G>A , CM000664.2:g.108378247G>A GRCh38
NC_000002.11:g.108994703G>A , CM000664.1:g.108994703G>A GRCh37
NC_000002.10:g.108361135G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-91G>A MANE Select ENSP00000272452.2:n.-91G>A
ENST00000272452.6:c.-91G>A ENSP00000272452.2:n.-91G>A
ENST00000409309.3:c.-91G>A ENSP00000387225.3:n.-91G>A
ENST00000494122.1:n.337G>A
NM_006588.2:c.-91G>A NP_006579.2:n.-91G>A
XM_005263919.2:c.-91G>A XP_005263976.1:n.-91G>A
NM_001321770.1:c.-91G>A NP_001308699.1:n.-91G>A
NM_006588.3:c.-91G>A NP_006579.2:n.-91G>A
NR_135776.1:n.337G>A
NR_135779.1:n.337G>A
NM_006588.4:c.-91G>A MANE Select NP_006579.2:n.-91G>A
NM_001321770.2:c.-91G>A NP_001308699.1:n.-91G>A
NR_135776.2:n.294G>A
NR_135779.2:n.294G>A
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