Canonical Allele Identifier: CA1172961733

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009383_67009384delinsAT , CM000663.2:g.67009383_67009384delinsAT	GRCh38
NC_000001.10:g.67475066_67475067delinsAT , CM000663.1:g.67475066_67475067delinsAT	GRCh37
NC_000001.9:g.67247654_67247655delinsAT	NCBI36
NG_012933.1:g.50014_50015delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-217_877-216delinsAT MANE Select	ENSP00000235345.5:n.877-217_877-216delinsAT
ENST00000235345.5:c.877-217_877-216delinsAT	ENSP00000235345.5:n.877-217_877-216delinsAT
NM_015139.2:c.877-217_877-216delinsAT	NP_055954.1:n.877-217_877-216delinsAT
XM_006710478.1:c.958-217_958-216delinsAT	XP_006710541.1:n.958-217_958-216delinsAT
XM_011541070.1:c.958-217_958-216delinsAT	XP_011539372.1:n.958-217_958-216delinsAT
XM_006710478.2:c.958-217_958-216delinsAT	XP_006710541.1:n.958-217_958-216delinsAT
XM_011541070.2:c.958-217_958-216delinsAT	XP_011539372.1:n.958-217_958-216delinsAT
XR_001737057.2:n.1461-217_1461-216delinsAT
XR_001737058.2:n.2246-217_2246-216delinsAT
NM_015139.3:c.877-217_877-216delinsAT MANE Select	NP_055954.1:n.877-217_877-216delinsAT