Canonical Allele Identifier: CA427904929

Gene: SULT1C4

Linked Data

• MyVariant Identifiers: chr2:g.108994943T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378487T>C , CM000664.2:g.108378487T>C	GRCh38
NC_000002.11:g.108994943T>C , CM000664.1:g.108994943T>C	GRCh37
NC_000002.10:g.108361375T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.150T>C MANE Select	ENSP00000272452.2:p.Ile50=
ENST00000272452.6:c.150T>C	ENSP00000272452.2:p.Ile50=
ENST00000409309.3:c.150T>C	ENSP00000387225.3:p.Ile50=
ENST00000494122.1:n.577T>C
NM_006588.2:c.150T>C	NP_006579.2:p.Ile50=
XM_005263919.2:c.150T>C	XP_005263976.1:p.Ile50=
NM_001321770.1:c.150T>C	NP_001308699.1:p.Ile50=
NM_006588.3:c.150T>C	NP_006579.2:p.Ile50=
NR_135776.1:n.577T>C
NR_135779.1:n.577T>C
XM_017003807.1:c.-171T>C	XP_016859296.1:n.-171T>C
NM_006588.4:c.150T>C MANE Select	NP_006579.2:p.Ile50=
NM_001321770.2:c.150T>C	NP_001308699.1:p.Ile50=
NR_135776.2:n.534T>C
NR_135779.2:n.534T>C