Canonical Allele Identifier: CA1172961614

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009037T= , CM000663.2:g.67009037T=	GRCh38
NC_000001.10:g.67474720T= , CM000663.1:g.67474720T=	GRCh37
NC_000001.9:g.67247308T=	NCBI36
NG_012933.1:g.50361A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.959+48A= MANE Select	ENSP00000235345.5:n.959+48A=
ENST00000235345.5:c.959+48A=	ENSP00000235345.5:n.959+48A=
NM_015139.2:c.959+48A=	NP_055954.1:n.959+48A=
XM_006710478.1:c.1040+48A=	XP_006710541.1:n.1040+48A=
XM_011541070.1:c.1040+48A=	XP_011539372.1:n.1040+48A=
XM_006710478.2:c.1040+48A=	XP_006710541.1:n.1040+48A=
XM_011541070.2:c.1040+48A=	XP_011539372.1:n.1040+48A=
XR_001737057.2:n.1543+48A=
XR_001737058.2:n.2328+48A=
NM_015139.3:c.959+48A= MANE Select	NP_055954.1:n.959+48A=