Canonical Allele Identifier: CA2646116174

Gene: SLC35D1

Linked Data

• gnomAD v4: 1-67009318-A-AGGGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009320_67009321insGTTGG , CM000663.2:g.67009320_67009321insGTTGG	GRCh38
NC_000001.10:g.67475003_67475004insGTTGG , CM000663.1:g.67475003_67475004insGTTGG	GRCh37
NC_000001.9:g.67247591_67247592insGTTGG	NCBI36
NG_012933.1:g.50079_50080insAACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-152_877-151insAACCC MANE Select	ENSP00000235345.5:n.877-152_877-151insAACCC
ENST00000235345.5:c.877-152_877-151insAACCC	ENSP00000235345.5:n.877-152_877-151insAACCC
NM_015139.2:c.877-152_877-151insAACCC	NP_055954.1:n.877-152_877-151insAACCC
XM_006710478.1:c.958-152_958-151insAACCC	XP_006710541.1:n.958-152_958-151insAACCC
XM_011541070.1:c.958-152_958-151insAACCC	XP_011539372.1:n.958-152_958-151insAACCC
XM_006710478.2:c.958-152_958-151insAACCC	XP_006710541.1:n.958-152_958-151insAACCC
XM_011541070.2:c.958-152_958-151insAACCC	XP_011539372.1:n.958-152_958-151insAACCC
XR_001737057.2:n.1461-152_1461-151insAACCC
XR_001737058.2:n.2246-152_2246-151insAACCC
NM_015139.3:c.877-152_877-151insAACCC MANE Select	NP_055954.1:n.877-152_877-151insAACCC