Canonical Allele Identifier: CA1172975749

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053902T= , CM000663.2:g.67053902T=	GRCh38
NC_000001.10:g.67519585T= , CM000663.1:g.67519585T=	GRCh37
NC_000001.9:g.67292173T=	NCBI36
NG_012933.1:g.5496A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.112A= MANE Select	ENSP00000235345.5:p.Thr38=
ENST00000235345.5:c.112A=	ENSP00000235345.5:p.Thr38=
NM_015139.2:c.112A=	NP_055954.1:p.Thr38=
XM_006710478.1:c.112A=	XP_006710541.1:p.Thr38=
XM_011541070.1:c.112A=	XP_011539372.1:p.Thr38=
XM_006710478.2:c.112A=	XP_006710541.1:p.Thr38=
XM_011541070.2:c.112A=	XP_011539372.1:p.Thr38=
XR_001737057.2:n.522A=
XR_001737058.2:n.515A=
NM_015139.3:c.112A= MANE Select	NP_055954.1:p.Thr38=