Canonical Allele Identifier: CA480520772

Gene: SLC35E3

Linked Data

• MyVariant Identifiers: chr12:g.69140361C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746581C>T , CM000674.2:g.68746581C>T	GRCh38
NC_000012.11:g.69140361C>T , CM000674.1:g.69140361C>T	GRCh37
NC_000012.10:g.67426628C>T	NCBI36
NG_046600.2:g.64631C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.447C>T
ENST00000398004.4:c.204C>T MANE Select	ENSP00000381089.2:p.Ala68=
ENST00000673712.1:c.204C>T	ENSP00000501065.1:p.Ala68=
ENST00000674096.1:c.204C>T	ENSP00000501130.1:p.Ala68=
ENST00000398004.3:c.204C>T	ENSP00000381089.2:p.Ala68=
NM_018656.2:c.204C>T	NP_061126.2:p.Ala68=
XM_005269006.2:c.204C>T	XP_005269063.1:p.Ala68=
NM_001354997.1:c.204C>T	NP_001341926.1:p.Ala68=
NM_001354998.1:c.204C>T	NP_001341927.1:p.Ala68=
NM_018656.3:c.204C>T	NP_061126.2:p.Ala68=
NR_149143.1:n.496C>T
NR_149144.1:n.496C>T
NM_001354997.3:c.204C>T	NP_001341926.1:p.Ala68=
NM_001354998.2:c.204C>T	NP_001341927.1:p.Ala68=
NM_018656.5:c.204C>T MANE Select	NP_061126.2:p.Ala68=
NR_149143.3:n.406C>T
NR_149144.3:n.406C>T