Canonical Allele Identifier: CA1172961698

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009293A= , CM000663.2:g.67009293A=	GRCh38
NC_000001.10:g.67474976A= , CM000663.1:g.67474976A=	GRCh37
NC_000001.9:g.67247564A=	NCBI36
NG_012933.1:g.50105T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-126T= MANE Select	ENSP00000235345.5:n.877-126T=
ENST00000235345.5:c.877-126T=	ENSP00000235345.5:n.877-126T=
NM_015139.2:c.877-126T=	NP_055954.1:n.877-126T=
XM_006710478.1:c.958-126T=	XP_006710541.1:n.958-126T=
XM_011541070.1:c.958-126T=	XP_011539372.1:n.958-126T=
XM_006710478.2:c.958-126T=	XP_006710541.1:n.958-126T=
XM_011541070.2:c.958-126T=	XP_011539372.1:n.958-126T=
XR_001737057.2:n.1461-126T=
XR_001737058.2:n.2246-126T=
NM_015139.3:c.877-126T= MANE Select	NP_055954.1:n.877-126T=