Canonical Allele Identifier: CA2044019977

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746573_68746575delinsATC , CM000674.2:g.68746573_68746575delinsATC	GRCh38
NC_000012.11:g.69140353_69140355delinsATC , CM000674.1:g.69140353_69140355delinsATC	GRCh37
NC_000012.10:g.67426620_67426622delinsATC	NCBI36
NG_046600.2:g.64623_64625delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.439_441delinsATC
ENST00000398004.4:c.196_198delinsATC MANE Select	ENSP00000381089.2:p.Ile66=
ENST00000673712.1:c.196_198delinsATC	ENSP00000501065.1:p.Ile66=
ENST00000674096.1:c.196_198delinsATC	ENSP00000501130.1:p.Ile66=
ENST00000398004.3:c.196_198delinsATC	ENSP00000381089.2:p.Ile66=
NM_018656.2:c.196_198delinsATC	NP_061126.2:p.Ile66=
XM_005269006.2:c.196_198delinsATC	XP_005269063.1:p.Ile66=
NM_001354997.1:c.196_198delinsATC	NP_001341926.1:p.Ile66=
NM_001354998.1:c.196_198delinsATC	NP_001341927.1:p.Ile66=
NM_018656.3:c.196_198delinsATC	NP_061126.2:p.Ile66=
NR_149143.1:n.488_490delinsATC
NR_149144.1:n.488_490delinsATC
NM_001354997.3:c.196_198delinsATC	NP_001341926.1:p.Ile66=
NM_001354998.2:c.196_198delinsATC	NP_001341927.1:p.Ile66=
NM_018656.5:c.196_198delinsATC MANE Select	NP_061126.2:p.Ile66=
NR_149143.3:n.398_400delinsATC
NR_149144.3:n.398_400delinsATC