Canonical Allele Identifier: CA348024385

Gene: SULT1C4

Linked Data

• gnomAD v4: 2-108378461-C-T
• MyVariant Identifiers: chr2:g.108994917C>T (hg19) ; chr2:g.108378461C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378461C>T , CM000664.2:g.108378461C>T	GRCh38
NC_000002.11:g.108994917C>T , CM000664.1:g.108994917C>T	GRCh37
NC_000002.10:g.108361349C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.124C>T MANE Select	ENSP00000272452.2:p.Gln42Ter
ENST00000272452.6:c.124C>T	ENSP00000272452.2:p.Gln42Ter
ENST00000409309.3:c.124C>T	ENSP00000387225.3:p.Gln42Ter
ENST00000494122.1:n.551C>T
NM_006588.2:c.124C>T	NP_006579.2:p.Gln42Ter
XM_005263919.2:c.124C>T	XP_005263976.1:p.Gln42Ter
NM_001321770.1:c.124C>T	NP_001308699.1:p.Gln42Ter
NM_006588.3:c.124C>T	NP_006579.2:p.Gln42Ter
NR_135776.1:n.551C>T
NR_135779.1:n.551C>T
XM_017003807.1:c.-197C>T	XP_016859296.1:n.-197C>T
NM_006588.4:c.124C>T MANE Select	NP_006579.2:p.Gln42Ter
NM_001321770.2:c.124C>T	NP_001308699.1:p.Gln42Ter
NR_135776.2:n.508C>T
NR_135779.2:n.508C>T