Canonical Allele Identifier: CA2660578711
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378290_108378291dup , CM000664.2:g.108378290_108378291dup GRCh38
NC_000002.11:g.108994746_108994747dup , CM000664.1:g.108994746_108994747dup GRCh37
NC_000002.10:g.108361178_108361179dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-48_-47dup MANE Select ENSP00000272452.2:n.-48_-47dup
ENST00000272452.6:c.-48_-47dup ENSP00000272452.2:n.-48_-47dup
ENST00000409309.3:c.-48_-47dup ENSP00000387225.3:n.-48_-47dup
ENST00000494122.1:n.380_381dup
NM_006588.2:c.-48_-47dup NP_006579.2:n.-48_-47dup
XM_005263919.2:c.-48_-47dup XP_005263976.1:n.-48_-47dup
NM_001321770.1:c.-48_-47dup NP_001308699.1:n.-48_-47dup
NM_006588.3:c.-48_-47dup NP_006579.2:n.-48_-47dup
NR_135776.1:n.380_381dup
NR_135779.1:n.380_381dup
NM_006588.4:c.-48_-47dup MANE Select NP_006579.2:n.-48_-47dup
NM_001321770.2:c.-48_-47dup NP_001308699.1:n.-48_-47dup
NR_135776.2:n.337_338dup
NR_135779.2:n.337_338dup