Canonical Allele Identifier: CA2044019788

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746484_68746486delinsATG , CM000674.2:g.68746484_68746486delinsATG	GRCh38
NC_000012.11:g.69140264_69140266delinsATG , CM000674.1:g.69140264_69140266delinsATG	GRCh37
NC_000012.10:g.67426531_67426533delinsATG	NCBI36
NG_046600.2:g.64534_64536delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.350_352delinsATG
ENST00000398004.4:c.107_109delinsATG MANE Select	ENSP00000381089.2:p.Tyr36=
ENST00000673712.1:c.107_109delinsATG	ENSP00000501065.1:p.Tyr36=
ENST00000674096.1:c.107_109delinsATG	ENSP00000501130.1:p.Tyr36=
ENST00000398004.3:c.107_109delinsATG	ENSP00000381089.2:p.Tyr36=
NM_018656.2:c.107_109delinsATG	NP_061126.2:p.Tyr36=
XM_005269006.2:c.107_109delinsATG	XP_005269063.1:p.Tyr36=
NM_001354997.1:c.107_109delinsATG	NP_001341926.1:p.Tyr36=
NM_001354998.1:c.107_109delinsATG	NP_001341927.1:p.Tyr36=
NM_018656.3:c.107_109delinsATG	NP_061126.2:p.Tyr36=
NR_149143.1:n.399_401delinsATG
NR_149144.1:n.399_401delinsATG
NM_001354997.3:c.107_109delinsATG	NP_001341926.1:p.Tyr36=
NM_001354998.2:c.107_109delinsATG	NP_001341927.1:p.Tyr36=
NM_018656.5:c.107_109delinsATG MANE Select	NP_061126.2:p.Tyr36=
NR_149143.3:n.309_311delinsATG
NR_149144.3:n.309_311delinsATG