Canonical Allele Identifier: CA1172961719

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009344G= , CM000663.2:g.67009344G=	GRCh38
NC_000001.10:g.67475027G= , CM000663.1:g.67475027G=	GRCh37
NC_000001.9:g.67247615G=	NCBI36
NG_012933.1:g.50054C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-177C= MANE Select	ENSP00000235345.5:n.877-177C=
ENST00000235345.5:c.877-177C=	ENSP00000235345.5:n.877-177C=
NM_015139.2:c.877-177C=	NP_055954.1:n.877-177C=
XM_006710478.1:c.958-177C=	XP_006710541.1:n.958-177C=
XM_011541070.1:c.958-177C=	XP_011539372.1:n.958-177C=
XM_006710478.2:c.958-177C=	XP_006710541.1:n.958-177C=
XM_011541070.2:c.958-177C=	XP_011539372.1:n.958-177C=
XR_001737057.2:n.1461-177C=
XR_001737058.2:n.2246-177C=
NM_015139.3:c.877-177C= MANE Select	NP_055954.1:n.877-177C=