Canonical Allele Identifier: CA53420431

Gene: SULT1C4

Linked Data

• MyVariant Identifiers: chr2:g.108994914_108994915insCCAAG (hg19) ; chr2:g.108378458_108378459insCCAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378458_108378459insCCAAG , CM000664.2:g.108378458_108378459insCCAAG	GRCh38
NC_000002.11:g.108994914_108994915insCCAAG , CM000664.1:g.108994914_108994915insCCAAG	GRCh37
NC_000002.10:g.108361346_108361347insCCAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.121_122insCCAAG MANE Select	ENSP00000272452.2:p.Phe41SerfsTer26
ENST00000272452.6:c.121_122insCCAAG	ENSP00000272452.2:p.Phe41SerfsTer26
ENST00000409309.3:c.121_122insCCAAG	ENSP00000387225.3:p.Phe41SerfsTer26
ENST00000494122.1:n.548_549insCCAAG
NM_006588.2:c.121_122insCCAAG	NP_006579.2:p.Phe41SerfsTer26
XM_005263919.2:c.121_122insCCAAG	XP_005263976.1:p.Phe41SerfsTer26
NM_001321770.1:c.121_122insCCAAG	NP_001308699.1:p.Phe41SerfsTer26
NM_006588.3:c.121_122insCCAAG	NP_006579.2:p.Phe41SerfsTer26
NR_135776.1:n.548_549insCCAAG
NR_135779.1:n.548_549insCCAAG
XM_017003807.1:c.-200_-199insCCAAG	XP_016859296.1:n.-200_-199insCCAAG
NM_006588.4:c.121_122insCCAAG MANE Select	NP_006579.2:p.Phe41SerfsTer26
NM_001321770.2:c.121_122insCCAAG	NP_001308699.1:p.Phe41SerfsTer26
NR_135776.2:n.505_506insCCAAG
NR_135779.2:n.505_506insCCAAG