Canonical Allele Identifier: CA754873123

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1221690781
• MyVariant Identifiers: chr2:g.108994763del (hg19) ; chr2:g.108378307del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378307del , CM000664.2:g.108378307del	GRCh38
NC_000002.11:g.108994763del , CM000664.1:g.108994763del	GRCh37
NC_000002.10:g.108361195del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.-31del MANE Select	ENSP00000272452.2:n.-31del
ENST00000272452.6:c.-31del	ENSP00000272452.2:n.-31del
ENST00000409309.3:c.-31del	ENSP00000387225.3:n.-31del
ENST00000494122.1:n.397del
NM_006588.2:c.-31del	NP_006579.2:n.-31del
XM_005263919.2:c.-31del	XP_005263976.1:n.-31del
NM_001321770.1:c.-31del	NP_001308699.1:n.-31del
NM_006588.3:c.-31del	NP_006579.2:n.-31del
NR_135776.1:n.397del
NR_135779.1:n.397del
NM_006588.4:c.-31del MANE Select	NP_006579.2:n.-31del
NM_001321770.2:c.-31del	NP_001308699.1:n.-31del
NR_135776.2:n.354del
NR_135779.2:n.354del