Canonical Allele Identifier: CA1278105122

Gene: SULT1C4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378313A= , CM000664.2:g.108378313A=	GRCh38
NC_000002.11:g.108994769A= , CM000664.1:g.108994769A=	GRCh37
NC_000002.10:g.108361201A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.-25A= MANE Select	ENSP00000272452.2:n.-25A=
ENST00000272452.6:c.-25A=	ENSP00000272452.2:n.-25A=
ENST00000409309.3:c.-25A=	ENSP00000387225.3:n.-25A=
ENST00000494122.1:n.403A=
NM_006588.2:c.-25A=	NP_006579.2:n.-25A=
XM_005263919.2:c.-25A=	XP_005263976.1:n.-25A=
NM_001321770.1:c.-25A=	NP_001308699.1:n.-25A=
NM_006588.3:c.-25A=	NP_006579.2:n.-25A=
NR_135776.1:n.403A=
NR_135779.1:n.403A=
NM_006588.4:c.-25A= MANE Select	NP_006579.2:n.-25A=
NM_001321770.2:c.-25A=	NP_001308699.1:n.-25A=
NR_135776.2:n.360A=
NR_135779.2:n.360A=