Canonical Allele Identifier: CA1172961689

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1667515909

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009270_67009273del , CM000663.2:g.67009270_67009273del	GRCh38
NC_000001.10:g.67474953_67474956del , CM000663.1:g.67474953_67474956del	GRCh37
NC_000001.9:g.67247541_67247544del	NCBI36
NG_012933.1:g.50128_50131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-103_877-100del MANE Select	ENSP00000235345.5:n.877-103_877-100del
ENST00000235345.5:c.877-103_877-100del	ENSP00000235345.5:n.877-103_877-100del
NM_015139.2:c.877-103_877-100del	NP_055954.1:n.877-103_877-100del
XM_006710478.1:c.958-103_958-100del	XP_006710541.1:n.958-103_958-100del
XM_011541070.1:c.958-103_958-100del	XP_011539372.1:n.958-103_958-100del
XM_006710478.2:c.958-103_958-100del	XP_006710541.1:n.958-103_958-100del
XM_011541070.2:c.958-103_958-100del	XP_011539372.1:n.958-103_958-100del
XR_001737057.2:n.1461-103_1461-100del
XR_001737058.2:n.2246-103_2246-100del
NM_015139.3:c.877-103_877-100del MANE Select	NP_055954.1:n.877-103_877-100del