Canonical Allele Identifier: CA238452499

Gene: SLC35E3

Linked Data

• dbSNP Id: rs985932585
• MyVariant Identifiers: chr12:g.69140153G>T (hg19) ; chr12:g.68746373G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746373G>T , CM000674.2:g.68746373G>T	GRCh38
NC_000012.11:g.69140153G>T , CM000674.1:g.69140153G>T	GRCh37
NC_000012.10:g.67426420G>T	NCBI36
NG_046600.2:g.64423G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.239G>T
ENST00000398004.4:c.-5G>T MANE Select	ENSP00000381089.2:n.-5G>T
ENST00000673712.1:c.-5G>T	ENSP00000501065.1:n.-5G>T
ENST00000674096.1:c.-5G>T	ENSP00000501130.1:n.-5G>T
ENST00000398004.3:c.-5G>T	ENSP00000381089.2:n.-5G>T
NM_018656.2:c.-5G>T	NP_061126.2:n.-5G>T
XM_005269006.2:c.-5G>T	XP_005269063.1:n.-5G>T
NM_001354997.1:c.-5G>T	NP_001341926.1:n.-5G>T
NM_001354998.1:c.-5G>T	NP_001341927.1:n.-5G>T
NM_018656.3:c.-5G>T	NP_061126.2:n.-5G>T
NR_149143.1:n.288G>T
NR_149144.1:n.288G>T
NM_001354997.3:c.-5G>T	NP_001341926.1:n.-5G>T
NM_001354998.2:c.-5G>T	NP_001341927.1:n.-5G>T
NM_018656.5:c.-5G>T MANE Select	NP_061126.2:n.-5G>T
NR_149143.3:n.198G>T
NR_149144.3:n.198G>T