Canonical Allele Identifier: CA12304025

Gene: SLC35F1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118256880G>A , CM000668.2:g.118256880G>A	GRCh38
NC_000006.11:g.118578043G>A , CM000668.1:g.118578043G>A	GRCh37
NC_000006.10:g.118684736G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360388.9:c.478-10115G>A MANE Select	ENSP00000353557.4:n.478-10115G>A
ENST00000360388.8:c.478-10115G>A	ENSP00000353557.4:n.478-10115G>A
ENST00000621341.1:c.301-10115G>A	ENSP00000484738.1:n.301-10115G>A
NM_001029858.3:c.478-10115G>A	NP_001025029.2:n.478-10115G>A
XM_005266865.3:c.478-10115G>A	XP_005266922.1:n.478-10115G>A
XM_005266865.4:c.478-10115G>A	XP_005266922.1:n.478-10115G>A
NM_001029858.4:c.478-10115G>A MANE Select	NP_001025029.2:n.478-10115G>A