Canonical Allele Identifier: CA1172975919

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054052C= , CM000663.2:g.67054052C=	GRCh38
NC_000001.10:g.67519735C= , CM000663.1:g.67519735C=	GRCh37
NC_000001.9:g.67292323C=	NCBI36
NG_012933.1:g.5346G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-39G= MANE Select	ENSP00000235345.5:n.-39G=
ENST00000235345.5:c.-39G=	ENSP00000235345.5:n.-39G=
NM_015139.2:c.-39G=	NP_055954.1:n.-39G=
XM_006710478.1:c.-39G=	XP_006710541.1:n.-39G=
XM_011541070.1:c.-39G=	XP_011539372.1:n.-39G=
XM_006710478.2:c.-39G=	XP_006710541.1:n.-39G=
XM_011541070.2:c.-39G=	XP_011539372.1:n.-39G=
XR_001737057.2:n.372G=
XR_001737058.2:n.365G=
NM_015139.3:c.-39G= MANE Select	NP_055954.1:n.-39G=