Canonical Allele Identifier: CA1278105161
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378405_108378406delinsAG , CM000664.2:g.108378405_108378406delinsAG GRCh38
NC_000002.11:g.108994861_108994862delinsAG , CM000664.1:g.108994861_108994862delinsAG GRCh37
NC_000002.10:g.108361293_108361294delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.68_69delinsAG MANE Select ENSP00000272452.2:p.Lys23=
ENST00000272452.6:c.68_69delinsAG ENSP00000272452.2:p.Lys23=
ENST00000409309.3:c.68_69delinsAG ENSP00000387225.3:p.Lys23=
ENST00000494122.1:n.495_496delinsAG
NM_006588.2:c.68_69delinsAG NP_006579.2:p.Lys23=
XM_005263919.2:c.68_69delinsAG XP_005263976.1:p.Lys23=
NM_001321770.1:c.68_69delinsAG NP_001308699.1:p.Lys23=
NM_006588.3:c.68_69delinsAG NP_006579.2:p.Lys23=
NR_135776.1:n.495_496delinsAG
NR_135779.1:n.495_496delinsAG
NM_006588.4:c.68_69delinsAG MANE Select NP_006579.2:p.Lys23=
NM_001321770.2:c.68_69delinsAG NP_001308699.1:p.Lys23=
NR_135776.2:n.452_453delinsAG
NR_135779.2:n.452_453delinsAG