Canonical Allele Identifier: CA412893991

Gene: SLC35A2

Linked Data

• gnomAD v4: X-48904763-C-G
• MyVariant Identifiers: chrX:g.48762040C>G (hg19) ; chrX:g.48904763C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904763C>G , CM000685.2:g.48904763C>G	GRCh38
NC_000023.10:g.48762040C>G , CM000685.1:g.48762040C>G	GRCh37
NC_000023.9:g.48646984C>G	NCBI36
NG_015967.1:g.11846C>G
NG_034300.1:g.12196G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.1146G>C MANE Select	ENSP00000247138.5:p.Thr382=
ENST00000247138.10:c.1146G>C	ENSP00000247138.5:p.Thr382=
ENST00000376515.8:c.484G>C	ENSP00000365698.3:p.Gly162Arg
ENST00000376521.6:c.1146G>C	ENSP00000365704.1:p.Thr382=
ENST00000376529.8:c.556G>C	ENSP00000365712.3:p.Gly186Arg
ENST00000413561.7:c.708G>C
ENST00000445167.7:c.556G>C	ENSP00000402726.2:p.Gly186Arg
ENST00000452555.7:c.1230G>C	ENSP00000416002.2:p.Thr410=
ENST00000616181.5:c.1185G>C	ENSP00000478617.1:p.Thr395=
ENST00000635285.1:c.1146G>C	ENSP00000489484.1:p.Thr382=
ENST00000635460.1:c.425-1298G>C
ENST00000635589.1:c.963G>C	ENSP00000489197.1:p.Thr321=
ENST00000635628.1:c.*1040G>C	ENSP00000489613.1:n.*1040G>C
NM_001032289.2:c.556G>C	NP_001027460.1:p.Gly186Arg
NM_001042498.2:c.1146G>C	NP_001035963.1:p.Thr382=
NM_001282647.1:c.556G>C	NP_001269576.1:p.Gly186Arg
NM_001282648.1:c.484G>C	NP_001269577.1:p.Gly162Arg
NM_001282649.1:c.963G>C	NP_001269578.1:p.Thr321=
NM_001282650.1:c.1185G>C	NP_001269579.1:p.Thr395=
NM_001282651.1:c.1230G>C	NP_001269580.1:p.Thr410=
NM_005660.2:c.1146G>C	NP_005651.1:p.Thr382=
NM_005660.3:c.1146G>C MANE Select	NP_005651.1:p.Thr382=
NM_001032289.3:c.556G>C	NP_001027460.1:p.Gly186Arg
NM_001042498.3:c.1146G>C	NP_001035963.1:p.Thr382=
NM_001282647.2:c.556G>C	NP_001269576.1:p.Gly186Arg
NM_001282649.2:c.963G>C	NP_001269578.1:p.Thr321=
NM_001282650.2:c.1185G>C	NP_001269579.1:p.Thr395=
NM_001282651.2:c.1230G>C	NP_001269580.1:p.Thr410=
NM_001282648.2:c.484G>C	NP_001269577.1:p.Gly162Arg