Canonical Allele Identifier: CA6678295

Gene: SLC35E3

Linked Data

• dbSNP Id: rs149163263
• ExAC: 12:69140505 C / T
• gnomAD v2: 12-69140505-C-T
• gnomAD v3: 12-68746725-C-T
• gnomAD v4: 12-68746725-C-T
• MyVariant Identifiers: chr12:g.69140505C>T (hg19) ; chr12:g.68746725C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746725C>T , CM000674.2:g.68746725C>T	GRCh38
NC_000012.11:g.69140505C>T , CM000674.1:g.69140505C>T	GRCh37
NC_000012.10:g.67426772C>T	NCBI36
NG_046600.2:g.64775C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.591C>T
ENST00000398004.4:c.348C>T MANE Select	ENSP00000381089.2:p.Ala116=
ENST00000673712.1:c.348C>T	ENSP00000501065.1:p.Ala116=
ENST00000674096.1:c.348C>T	ENSP00000501130.1:p.Ala116=
ENST00000398004.3:c.348C>T	ENSP00000381089.2:p.Ala116=
NM_018656.2:c.348C>T	NP_061126.2:p.Ala116=
XM_005269006.2:c.348C>T	XP_005269063.1:p.Ala116=
NM_001354997.1:c.348C>T	NP_001341926.1:p.Ala116=
NM_001354998.1:c.348C>T	NP_001341927.1:p.Ala116=
NM_018656.3:c.348C>T	NP_061126.2:p.Ala116=
NR_149143.1:n.640C>T
NR_149144.1:n.640C>T
NM_001354997.3:c.348C>T	NP_001341926.1:p.Ala116=
NM_001354998.2:c.348C>T	NP_001341927.1:p.Ala116=
NM_018656.5:c.348C>T MANE Select	NP_061126.2:p.Ala116=
NR_149143.3:n.550C>T
NR_149144.3:n.550C>T