Canonical Allele Identifier: CA222949

Gene: SLC35A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87473010G>T , CM000668.2:g.87473010G>T	GRCh38
NC_000006.11:g.88182728G>T , CM000668.1:g.88182728G>T	GRCh37
NC_000006.10:g.88239447G>T	NCBI36
NG_016207.1:g.5086G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369552.9:c.7G>T MANE Select	ENSP00000358565.4:p.Ala3Ser
ENST00000369552.8:c.7G>T	ENSP00000358565.4:p.Ala3Ser
ENST00000369556.7:c.7G>T	ENSP00000358569.3:p.Ala3Ser
ENST00000369557.9:c.7G>T	ENSP00000358570.5:p.Ala3Ser
ENST00000464978.5:n.91+2297G>T
ENST00000506888.5:n.556-4352G>T
ENST00000507897.5:c.*61-4352G>T	ENSP00000426769.1:n.*61-4352G>T
ENST00000513191.1:n.510-4352G>T
ENST00000544441.4:c.7G>T	ENSP00000438603.2:p.Ala3Ser
NM_001168398.1:c.7G>T	NP_001161870.1:p.Ala3Ser
NM_006416.4:c.7G>T	NP_006407.1:p.Ala3Ser
NM_006416.5:c.7G>T MANE Select	NP_006407.1:p.Ala3Ser
NM_001168398.2:c.7G>T	NP_001161870.1:p.Ala3Ser