Canonical Allele Identifier: CA1172976013

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054113G= , CM000663.2:g.67054113G=	GRCh38
NC_000001.10:g.67519796G= , CM000663.1:g.67519796G=	GRCh37
NC_000001.9:g.67292384G=	NCBI36
NG_012933.1:g.5285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-100C= MANE Select	ENSP00000235345.5:n.-100C=
NM_015139.2:c.-100C=	NP_055954.1:n.-100C=
XM_006710478.1:c.-100C=	XP_006710541.1:n.-100C=
XM_011541070.1:c.-100C=	XP_011539372.1:n.-100C=
XM_006710478.2:c.-100C=	XP_006710541.1:n.-100C=
XM_011541070.2:c.-100C=	XP_011539372.1:n.-100C=
XR_001737057.2:n.311C=
XR_001737058.2:n.304C=
NM_015139.3:c.-100C= MANE Select	NP_055954.1:n.-100C=