Canonical Allele Identifier: CA738095344

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1157185924
• gnomAD v3: 1-67009220-A-AAT
• gnomAD v4: 1-67009220-A-AAT
• MyVariant Identifiers: chr1:g.67474903_67474904insAT (hg19) ; chr1:g.67009220_67009221insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009228_67009229dup , CM000663.2:g.67009228_67009229dup	GRCh38
NC_000001.10:g.67474911_67474912dup , CM000663.1:g.67474911_67474912dup	GRCh37
NC_000001.9:g.67247499_67247500dup	NCBI36
NG_012933.1:g.50176_50177dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-55_877-54dup MANE Select	ENSP00000235345.5:n.877-55_877-54dup
ENST00000235345.5:c.877-55_877-54dup	ENSP00000235345.5:n.877-55_877-54dup
NM_015139.2:c.877-55_877-54dup	NP_055954.1:n.877-55_877-54dup
XM_006710478.1:c.958-55_958-54dup	XP_006710541.1:n.958-55_958-54dup
XM_011541070.1:c.958-55_958-54dup	XP_011539372.1:n.958-55_958-54dup
XM_006710478.2:c.958-55_958-54dup	XP_006710541.1:n.958-55_958-54dup
XM_011541070.2:c.958-55_958-54dup	XP_011539372.1:n.958-55_958-54dup
XR_001737057.2:n.1461-55_1461-54dup
XR_001737058.2:n.2246-55_2246-54dup
NM_015139.3:c.877-55_877-54dup MANE Select	NP_055954.1:n.877-55_877-54dup