Canonical Allele Identifier: CA1278105172

Gene: SULT1C4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378428A= , CM000664.2:g.108378428A=	GRCh38
NC_000002.11:g.108994884A= , CM000664.1:g.108994884A=	GRCh37
NC_000002.10:g.108361316A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.91A= MANE Select	ENSP00000272452.2:p.Thr31=
ENST00000272452.6:c.91A=	ENSP00000272452.2:p.Thr31=
ENST00000409309.3:c.91A=	ENSP00000387225.3:p.Thr31=
ENST00000494122.1:n.518A=
NM_006588.2:c.91A=	NP_006579.2:p.Thr31=
XM_005263919.2:c.91A=	XP_005263976.1:p.Thr31=
NM_001321770.1:c.91A=	NP_001308699.1:p.Thr31=
NM_006588.3:c.91A=	NP_006579.2:p.Thr31=
NR_135776.1:n.518A=
NR_135779.1:n.518A=
XM_017003807.1:c.-230A=	XP_016859296.1:n.-230A=
NM_006588.4:c.91A= MANE Select	NP_006579.2:p.Thr31=
NM_001321770.2:c.91A=	NP_001308699.1:p.Thr31=
NR_135776.2:n.475A=
NR_135779.2:n.475A=