Canonical Allele Identifier: CA412894102

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762081G>T (hg19) ; chrX:g.48904804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904804G>T , CM000685.2:g.48904804G>T	GRCh38
NC_000023.10:g.48762081G>T , CM000685.1:g.48762081G>T	GRCh37
NC_000023.9:g.48647025G>T	NCBI36
NG_015967.1:g.11887G>T
NG_034300.1:g.12155C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.1105C>A MANE Select	ENSP00000247138.5:p.Pro369Thr
ENST00000247138.10:c.1105C>A	ENSP00000247138.5:p.Pro369Thr
ENST00000376515.8:c.443C>A	ENSP00000365698.3:p.Thr148Asn
ENST00000376521.6:c.1105C>A	ENSP00000365704.1:p.Pro369Thr
ENST00000376529.8:c.515C>A	ENSP00000365712.3:p.Thr172Asn
ENST00000413561.7:c.667C>A
ENST00000445167.7:c.515C>A	ENSP00000402726.2:p.Thr172Asn
ENST00000452555.7:c.1189C>A	ENSP00000416002.2:p.Pro397Thr
ENST00000616181.5:c.1144C>A	ENSP00000478617.1:p.Pro382Thr
ENST00000635285.1:c.1105C>A	ENSP00000489484.1:p.Pro369Thr
ENST00000635460.1:c.425-1339C>A
ENST00000635589.1:c.922C>A	ENSP00000489197.1:p.Pro308Thr
ENST00000635628.1:c.*999C>A	ENSP00000489613.1:n.*999C>A
NM_001032289.2:c.515C>A	NP_001027460.1:p.Thr172Asn
NM_001042498.2:c.1105C>A	NP_001035963.1:p.Pro369Thr
NM_001282647.1:c.515C>A	NP_001269576.1:p.Thr172Asn
NM_001282648.1:c.443C>A	NP_001269577.1:p.Thr148Asn
NM_001282649.1:c.922C>A	NP_001269578.1:p.Pro308Thr
NM_001282650.1:c.1144C>A	NP_001269579.1:p.Pro382Thr
NM_001282651.1:c.1189C>A	NP_001269580.1:p.Pro397Thr
NM_005660.2:c.1105C>A	NP_005651.1:p.Pro369Thr
NM_005660.3:c.1105C>A MANE Select	NP_005651.1:p.Pro369Thr
NM_001032289.3:c.515C>A	NP_001027460.1:p.Thr172Asn
NM_001042498.3:c.1105C>A	NP_001035963.1:p.Pro369Thr
NM_001282647.2:c.515C>A	NP_001269576.1:p.Thr172Asn
NM_001282649.2:c.922C>A	NP_001269578.1:p.Pro308Thr
NM_001282650.2:c.1144C>A	NP_001269579.1:p.Pro382Thr
NM_001282651.2:c.1189C>A	NP_001269580.1:p.Pro397Thr
NM_001282648.2:c.443C>A	NP_001269577.1:p.Thr148Asn