Canonical Allele Identifier: CA348024431

Gene: SULT1C4

Linked Data

• gnomAD v4: 2-108378482-C-A
• MyVariant Identifiers: chr2:g.108994938C>A (hg19) ; chr2:g.108378482C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378482C>A , CM000664.2:g.108378482C>A	GRCh38
NC_000002.11:g.108994938C>A , CM000664.1:g.108994938C>A	GRCh37
NC_000002.10:g.108361370C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.145C>A MANE Select	ENSP00000272452.2:p.Leu49Ile
ENST00000272452.6:c.145C>A	ENSP00000272452.2:p.Leu49Ile
ENST00000409309.3:c.145C>A	ENSP00000387225.3:p.Leu49Ile
ENST00000494122.1:n.572C>A
NM_006588.2:c.145C>A	NP_006579.2:p.Leu49Ile
XM_005263919.2:c.145C>A	XP_005263976.1:p.Leu49Ile
NM_001321770.1:c.145C>A	NP_001308699.1:p.Leu49Ile
NM_006588.3:c.145C>A	NP_006579.2:p.Leu49Ile
NR_135776.1:n.572C>A
NR_135779.1:n.572C>A
XM_017003807.1:c.-176C>A	XP_016859296.1:n.-176C>A
NM_006588.4:c.145C>A MANE Select	NP_006579.2:p.Leu49Ile
NM_001321770.2:c.145C>A	NP_001308699.1:p.Leu49Ile
NR_135776.2:n.529C>A
NR_135779.2:n.529C>A