Canonical Allele Identifier: CA348024428

Gene: SULT1C4

Linked Data

• MyVariant Identifiers: chr2:g.108994936T>A (hg19) ; chr2:g.108378480T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378480T>A , CM000664.2:g.108378480T>A	GRCh38
NC_000002.11:g.108994936T>A , CM000664.1:g.108994936T>A	GRCh37
NC_000002.10:g.108361368T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.143T>A MANE Select	ENSP00000272452.2:p.Leu48Gln
ENST00000272452.6:c.143T>A	ENSP00000272452.2:p.Leu48Gln
ENST00000409309.3:c.143T>A	ENSP00000387225.3:p.Leu48Gln
ENST00000494122.1:n.570T>A
NM_006588.2:c.143T>A	NP_006579.2:p.Leu48Gln
XM_005263919.2:c.143T>A	XP_005263976.1:p.Leu48Gln
NM_001321770.1:c.143T>A	NP_001308699.1:p.Leu48Gln
NM_006588.3:c.143T>A	NP_006579.2:p.Leu48Gln
NR_135776.1:n.570T>A
NR_135779.1:n.570T>A
XM_017003807.1:c.-178T>A	XP_016859296.1:n.-178T>A
NM_006588.4:c.143T>A MANE Select	NP_006579.2:p.Leu48Gln
NM_001321770.2:c.143T>A	NP_001308699.1:p.Leu48Gln
NR_135776.2:n.527T>A
NR_135779.2:n.527T>A