Canonical Allele Identifier: CA2044020209

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746716_68746719delinsGATC , CM000674.2:g.68746716_68746719delinsGATC	GRCh38
NC_000012.11:g.69140496_69140499delinsGATC , CM000674.1:g.69140496_69140499delinsGATC	GRCh37
NC_000012.10:g.67426763_67426766delinsGATC	NCBI36
NG_046600.2:g.64766_64769delinsGATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.582_585delinsGATC
ENST00000398004.4:c.339_342delinsGATC MANE Select	ENSP00000381089.2:p.Val113=
ENST00000673712.1:c.339_342delinsGATC	ENSP00000501065.1:p.Val113=
ENST00000674096.1:c.339_342delinsGATC	ENSP00000501130.1:p.Val113=
ENST00000398004.3:c.339_342delinsGATC	ENSP00000381089.2:p.Val113=
NM_018656.2:c.339_342delinsGATC	NP_061126.2:p.Val113=
XM_005269006.2:c.339_342delinsGATC	XP_005269063.1:p.Val113=
NM_001354997.1:c.339_342delinsGATC	NP_001341926.1:p.Val113=
NM_001354998.1:c.339_342delinsGATC	NP_001341927.1:p.Val113=
NM_018656.3:c.339_342delinsGATC	NP_061126.2:p.Val113=
NR_149143.1:n.631_634delinsGATC
NR_149144.1:n.631_634delinsGATC
NM_001354997.3:c.339_342delinsGATC	NP_001341926.1:p.Val113=
NM_001354998.2:c.339_342delinsGATC	NP_001341927.1:p.Val113=
NM_018656.5:c.339_342delinsGATC MANE Select	NP_061126.2:p.Val113=
NR_149143.3:n.541_544delinsGATC
NR_149144.3:n.541_544delinsGATC