Canonical Allele Identifier: CA10406074
Gene: SLC35A2 HGNC NCBI

Linked Data

dbSNP Id: rs782526017
gnomAD v2: X-48762165-G-C
gnomAD v4: X-48904888-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48904888G>C , CM000685.2:g.48904888G>C GRCh38
NC_000023.10:g.48762165G>C , CM000685.1:g.48762165G>C GRCh37
NC_000023.9:g.48647109G>C NCBI36
NG_015967.1:g.11971G>C
NG_034300.1:g.12071C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000247138.11:c.1021C>G MANE Select ENSP00000247138.5:p.Pro341Ala
ENST00000247138.10:c.1021C>G ENSP00000247138.5:p.Pro341Ala
ENST00000376515.8:c.359C>G ENSP00000365698.3:p.Ser120Cys
ENST00000376521.6:c.1021C>G ENSP00000365704.1:p.Pro341Ala
ENST00000376529.8:c.431C>G ENSP00000365712.3:p.Ser144Cys
ENST00000413561.7:c.583C>G
ENST00000445167.7:c.431C>G ENSP00000402726.2:p.Ser144Cys
ENST00000452555.7:c.1105C>G ENSP00000416002.2:p.Pro369Ala
ENST00000616181.5:c.1060C>G ENSP00000478617.1:p.Pro354Ala
ENST00000635285.1:c.1021C>G ENSP00000489484.1:p.Pro341Ala
ENST00000635460.1:c.425-1423C>G
ENST00000635589.1:c.838C>G ENSP00000489197.1:p.Pro280Ala
ENST00000635628.1:c.*915C>G ENSP00000489613.1:n.*915C>G
NM_001032289.2:c.431C>G NP_001027460.1:p.Ser144Cys
NM_001042498.2:c.1021C>G NP_001035963.1:p.Pro341Ala
NM_001282647.1:c.431C>G NP_001269576.1:p.Ser144Cys
NM_001282648.1:c.359C>G NP_001269577.1:p.Ser120Cys
NM_001282649.1:c.838C>G NP_001269578.1:p.Pro280Ala
NM_001282650.1:c.1060C>G NP_001269579.1:p.Pro354Ala
NM_001282651.1:c.1105C>G NP_001269580.1:p.Pro369Ala
NM_005660.2:c.1021C>G NP_005651.1:p.Pro341Ala
NM_005660.3:c.1021C>G MANE Select NP_005651.1:p.Pro341Ala
NM_001032289.3:c.431C>G NP_001027460.1:p.Ser144Cys
NM_001042498.3:c.1021C>G NP_001035963.1:p.Pro341Ala
NM_001282647.2:c.431C>G NP_001269576.1:p.Ser144Cys
NM_001282649.2:c.838C>G NP_001269578.1:p.Pro280Ala
NM_001282650.2:c.1060C>G NP_001269579.1:p.Pro354Ala
NM_001282651.2:c.1105C>G NP_001269580.1:p.Pro369Ala
NM_001282648.2:c.359C>G NP_001269577.1:p.Ser120Cys