Canonical Allele Identifier: CA427904883

Gene: SULT1C4

Linked Data

• gnomAD v4: 2-108378406-G-A
• MyVariant Identifiers: chr2:g.108994862G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378406G>A , CM000664.2:g.108378406G>A	GRCh38
NC_000002.11:g.108994862G>A , CM000664.1:g.108994862G>A	GRCh37
NC_000002.10:g.108361294G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.69G>A MANE Select	ENSP00000272452.2:p.Lys23=
ENST00000272452.6:c.69G>A	ENSP00000272452.2:p.Lys23=
ENST00000409309.3:c.69G>A	ENSP00000387225.3:p.Lys23=
ENST00000494122.1:n.496G>A
NM_006588.2:c.69G>A	NP_006579.2:p.Lys23=
XM_005263919.2:c.69G>A	XP_005263976.1:p.Lys23=
NM_001321770.1:c.69G>A	NP_001308699.1:p.Lys23=
NM_006588.3:c.69G>A	NP_006579.2:p.Lys23=
NR_135776.1:n.496G>A
NR_135779.1:n.496G>A
NM_006588.4:c.69G>A MANE Select	NP_006579.2:p.Lys23=
NM_001321770.2:c.69G>A	NP_001308699.1:p.Lys23=
NR_135776.2:n.453G>A
NR_135779.2:n.453G>A