Canonical Allele Identifier: CA1278105149

Gene: SULT1C4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378377_108378378delinsAC , CM000664.2:g.108378377_108378378delinsAC	GRCh38
NC_000002.11:g.108994833_108994834delinsAC , CM000664.1:g.108994833_108994834delinsAC	GRCh37
NC_000002.10:g.108361265_108361266delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.40_41delinsAC MANE Select	ENSP00000272452.2:p.Thr14=
ENST00000272452.6:c.40_41delinsAC	ENSP00000272452.2:p.Thr14=
ENST00000409309.3:c.40_41delinsAC	ENSP00000387225.3:p.Thr14=
ENST00000494122.1:n.467_468delinsAC
NM_006588.2:c.40_41delinsAC	NP_006579.2:p.Thr14=
XM_005263919.2:c.40_41delinsAC	XP_005263976.1:p.Thr14=
NM_001321770.1:c.40_41delinsAC	NP_001308699.1:p.Thr14=
NM_006588.3:c.40_41delinsAC	NP_006579.2:p.Thr14=
NR_135776.1:n.467_468delinsAC
NR_135779.1:n.467_468delinsAC
NM_006588.4:c.40_41delinsAC MANE Select	NP_006579.2:p.Thr14=
NM_001321770.2:c.40_41delinsAC	NP_001308699.1:p.Thr14=
NR_135776.2:n.424_425delinsAC
NR_135779.2:n.424_425delinsAC