Canonical Allele Identifier: CA412896733

Gene: SLC35A2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48906491A>C , CM000685.2:g.48906491A>C	GRCh38
NC_000023.10:g.48763768A>C , CM000685.1:g.48763768A>C	GRCh37
NC_000023.9:g.48648712A>C	NCBI36
NG_034300.1:g.10468T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.327T>G MANE Select	ENSP00000247138.5:p.Tyr109Ter
ENST00000247138.10:c.327T>G	ENSP00000247138.5:p.Tyr109Ter
ENST00000376512.2:c.327T>G	ENSP00000365695.1:p.Tyr109Ter
ENST00000376515.8:c.255T>G	ENSP00000365698.3:p.Tyr85Ter
ENST00000376521.6:c.327T>G	ENSP00000365704.1:p.Tyr109Ter
ENST00000376529.8:c.327T>G	ENSP00000365712.3:p.Tyr109Ter
ENST00000413561.7:c.112T>G
ENST00000445167.7:c.327T>G	ENSP00000402726.2:p.Tyr109Ter
ENST00000446885.1:c.111T>G	ENSP00000415518.1:p.Tyr37Ter
ENST00000452555.7:c.411T>G	ENSP00000416002.2:p.Tyr137Ter
ENST00000616181.5:c.366T>G	ENSP00000478617.1:p.Tyr122Ter
ENST00000634461.1:c.144T>G	ENSP00000489440.1:p.Tyr48Ter
ENST00000634665.1:c.292T>G	ENSP00000489356.1:p.Cys98Gly
ENST00000635015.1:c.366T>G	ENSP00000489089.1:p.Tyr122Ter
ENST00000635238.1:c.288T>G	ENSP00000489515.1:p.Tyr96Ter
ENST00000635285.1:c.327T>G	ENSP00000489484.1:p.Tyr109Ter
ENST00000635460.1:c.325T>G
ENST00000635589.1:c.144T>G	ENSP00000489197.1:p.Tyr48Ter
ENST00000635628.1:c.*221T>G	ENSP00000489613.1:n.*221T>G
NM_001032289.2:c.327T>G	NP_001027460.1:p.Tyr109Ter
NM_001042498.2:c.327T>G	NP_001035963.1:p.Tyr109Ter
NM_001282647.1:c.327T>G	NP_001269576.1:p.Tyr109Ter
NM_001282648.1:c.255T>G	NP_001269577.1:p.Tyr85Ter
NM_001282649.1:c.144T>G	NP_001269578.1:p.Tyr48Ter
NM_001282650.1:c.366T>G	NP_001269579.1:p.Tyr122Ter
NM_001282651.1:c.411T>G	NP_001269580.1:p.Tyr137Ter
NM_005660.2:c.327T>G	NP_005651.1:p.Tyr109Ter
NM_005660.3:c.327T>G MANE Select	NP_005651.1:p.Tyr109Ter
NM_001032289.3:c.327T>G	NP_001027460.1:p.Tyr109Ter
NM_001042498.3:c.327T>G	NP_001035963.1:p.Tyr109Ter
NM_001282647.2:c.327T>G	NP_001269576.1:p.Tyr109Ter
NM_001282649.2:c.144T>G	NP_001269578.1:p.Tyr48Ter
NM_001282650.2:c.366T>G	NP_001269579.1:p.Tyr122Ter
NM_001282651.2:c.411T>G	NP_001269580.1:p.Tyr137Ter
NM_001282648.2:c.255T>G	NP_001269577.1:p.Tyr85Ter