Canonical Allele Identifier: CA1172975692

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053842C= , CM000663.2:g.67053842C=	GRCh38
NC_000001.10:g.67519525C= , CM000663.1:g.67519525C=	GRCh37
NC_000001.9:g.67292113C=	NCBI36
NG_012933.1:g.5556G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.172G= MANE Select	ENSP00000235345.5:p.Val58=
ENST00000235345.5:c.172G=	ENSP00000235345.5:p.Val58=
NM_015139.2:c.172G=	NP_055954.1:p.Val58=
XM_006710478.1:c.172G=	XP_006710541.1:p.Val58=
XM_011541070.1:c.172G=	XP_011539372.1:p.Val58=
XM_006710478.2:c.172G=	XP_006710541.1:p.Val58=
XM_011541070.2:c.172G=	XP_011539372.1:p.Val58=
XR_001737057.2:n.582G=
XR_001737058.2:n.575G=
NM_015139.3:c.172G= MANE Select	NP_055954.1:p.Val58=