Canonical Allele Identifier: CA1143622940

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054047C= , CM000663.2:g.67054047C=	GRCh38
NC_000001.10:g.67519730C= , CM000663.1:g.67519730C=	GRCh37
NC_000001.9:g.67292318C=	NCBI36
NG_012933.1:g.5351G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-34G= MANE Select	ENSP00000235345.5:n.-34G=
ENST00000235345.5:c.-34G=	ENSP00000235345.5:n.-34G=
NM_015139.2:c.-34G=	NP_055954.1:n.-34G=
XM_006710478.1:c.-34G=	XP_006710541.1:n.-34G=
XM_011541070.1:c.-34G=	XP_011539372.1:n.-34G=
XM_006710478.2:c.-34G=	XP_006710541.1:n.-34G=
XM_011541070.2:c.-34G=	XP_011539372.1:n.-34G=
XR_001737057.2:n.377G=
XR_001737058.2:n.370G=
NM_015139.3:c.-34G= MANE Select	NP_055954.1:n.-34G=