Canonical Allele Identifier: CA1278105198

Gene: SULT1C4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378496T= , CM000664.2:g.108378496T=	GRCh38
NC_000002.11:g.108994952T= , CM000664.1:g.108994952T=	GRCh37
NC_000002.10:g.108361384T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.159T= MANE Select	ENSP00000272452.2:p.Tyr53=
ENST00000272452.6:c.159T=	ENSP00000272452.2:p.Tyr53=
ENST00000409309.3:c.159T=	ENSP00000387225.3:p.Tyr53=
ENST00000494122.1:n.586T=
NM_006588.2:c.159T=	NP_006579.2:p.Tyr53=
XM_005263919.2:c.159T=	XP_005263976.1:p.Tyr53=
NM_001321770.1:c.159T=	NP_001308699.1:p.Tyr53=
NM_006588.3:c.159T=	NP_006579.2:p.Tyr53=
NR_135776.1:n.586T=
NR_135779.1:n.586T=
XM_017003807.1:c.-162T=	XP_016859296.1:n.-162T=
NM_006588.4:c.159T= MANE Select	NP_006579.2:p.Tyr53=
NM_001321770.2:c.159T=	NP_001308699.1:p.Tyr53=
NR_135776.2:n.543T=
NR_135779.2:n.543T=