Canonical Allele Identifier: CA348024300
Gene: SULT1C4 HGNC NCBI

Linked Data

COSMIC: COSM3565074
MyVariant Identifiers: chr2:g.108994898G>A (hg19) chr2:g.108378442G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378442G>A , CM000664.2:g.108378442G>A GRCh38
NC_000002.11:g.108994898G>A , CM000664.1:g.108994898G>A GRCh37
NC_000002.10:g.108361330G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.105G>A MANE Select ENSP00000272452.2:p.Trp35Ter
ENST00000272452.6:c.105G>A ENSP00000272452.2:p.Trp35Ter
ENST00000409309.3:c.105G>A ENSP00000387225.3:p.Trp35Ter
ENST00000494122.1:n.532G>A
NM_006588.2:c.105G>A NP_006579.2:p.Trp35Ter
XM_005263919.2:c.105G>A XP_005263976.1:p.Trp35Ter
NM_001321770.1:c.105G>A NP_001308699.1:p.Trp35Ter
NM_006588.3:c.105G>A NP_006579.2:p.Trp35Ter
NR_135776.1:n.532G>A
NR_135779.1:n.532G>A
XM_017003807.1:c.-216G>A XP_016859296.1:n.-216G>A
NM_006588.4:c.105G>A MANE Select NP_006579.2:p.Trp35Ter
NM_001321770.2:c.105G>A NP_001308699.1:p.Trp35Ter
NR_135776.2:n.489G>A
NR_135779.2:n.489G>A
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