Canonical Allele Identifier: CA1968692230

Gene: SLC35C1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805753C= , CM000673.2:g.45805753C=	GRCh38
NC_000011.9:g.45827304C= , CM000673.1:g.45827304C=	GRCh37
NC_000011.8:g.45783880C=	NCBI36
NG_009875.1:g.6682C= , LRG_107:g.6682C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.-31-57C=	ENSP00000432145.2:n.-31-57C=
ENST00000314134.4:c.-49C= MANE Select	ENSP00000313318.3:n.-49C=
ENST00000314134.3:c.-49C=	ENSP00000313318.3:n.-49C=
ENST00000442528.2:c.-31-57C=	ENSP00000412408.2:n.-31-57C=
ENST00000526817.1:c.-31-57C=	ENSP00000432145.1:n.-31-57C=
ENST00000530471.1:c.-31-57C=	ENSP00000432669.1:n.-31-57C=
NM_001145265.1:c.-31-57C=	NP_001138737.1:n.-31-57C=
NM_001145266.1:c.-31-57C=	NP_001138738.1:n.-31-57C=
NM_018389.4:c.-49C= , LRG_107t1:c.-49C=	NP_060859.4:n.-49C=
XM_011520203.1:c.-49C=	XP_011518505.1:n.-49C=
XM_011520203.3:c.-49C=	XP_011518505.1:n.-49C=
NM_001145265.2:c.-31-57C=	NP_001138737.1:n.-31-57C=
NM_018389.5:c.-49C= MANE Select	NP_060859.4:n.-49C=