Canonical Allele Identifier: CA427904909

Gene: SULT1C4

Linked Data

• MyVariant Identifiers: chr2:g.108994907C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378451C>A , CM000664.2:g.108378451C>A	GRCh38
NC_000002.11:g.108994907C>A , CM000664.1:g.108994907C>A	GRCh37
NC_000002.10:g.108361339C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.114C>A MANE Select	ENSP00000272452.2:p.Ile38=
ENST00000272452.6:c.114C>A	ENSP00000272452.2:p.Ile38=
ENST00000409309.3:c.114C>A	ENSP00000387225.3:p.Ile38=
ENST00000494122.1:n.541C>A
NM_006588.2:c.114C>A	NP_006579.2:p.Ile38=
XM_005263919.2:c.114C>A	XP_005263976.1:p.Ile38=
NM_001321770.1:c.114C>A	NP_001308699.1:p.Ile38=
NM_006588.3:c.114C>A	NP_006579.2:p.Ile38=
NR_135776.1:n.541C>A
NR_135779.1:n.541C>A
XM_017003807.1:c.-207C>A	XP_016859296.1:n.-207C>A
NM_006588.4:c.114C>A MANE Select	NP_006579.2:p.Ile38=
NM_001321770.2:c.114C>A	NP_001308699.1:p.Ile38=
NR_135776.2:n.498C>A
NR_135779.2:n.498C>A