Canonical Allele Identifier: CA1278105181

Gene: SULT1C4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378457C= , CM000664.2:g.108378457C=	GRCh38
NC_000002.11:g.108994913C= , CM000664.1:g.108994913C=	GRCh37
NC_000002.10:g.108361345C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.120C= MANE Select	ENSP00000272452.2:p.Asn40=
ENST00000272452.6:c.120C=	ENSP00000272452.2:p.Asn40=
ENST00000409309.3:c.120C=	ENSP00000387225.3:p.Asn40=
ENST00000494122.1:n.547C=
NM_006588.2:c.120C=	NP_006579.2:p.Asn40=
XM_005263919.2:c.120C=	XP_005263976.1:p.Asn40=
NM_001321770.1:c.120C=	NP_001308699.1:p.Asn40=
NM_006588.3:c.120C=	NP_006579.2:p.Asn40=
NR_135776.1:n.547C=
NR_135779.1:n.547C=
XM_017003807.1:c.-201C=	XP_016859296.1:n.-201C=
NM_006588.4:c.120C= MANE Select	NP_006579.2:p.Asn40=
NM_001321770.2:c.120C=	NP_001308699.1:p.Asn40=
NR_135776.2:n.504C=
NR_135779.2:n.504C=