Canonical Allele Identifier: CA474036818

Gene: SLC35C1

Linked Data

• MyVariant Identifiers: chr11:g.45827862C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806311C>G , CM000673.2:g.45806311C>G	GRCh38
NC_000011.9:g.45827862C>G , CM000673.1:g.45827862C>G	GRCh37
NC_000011.8:g.45784438C>G	NCBI36
NG_009875.1:g.7240C>G , LRG_107:g.7240C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000526817.2:c.471C>G	ENSP00000432145.2:p.Ala157=
ENST00000314134.4:c.510C>G MANE Select	ENSP00000313318.3:p.Ala170=
ENST00000314134.3:c.510C>G	ENSP00000313318.3:p.Ala170=
ENST00000442528.2:c.471C>G	ENSP00000412408.2:p.Ala157=
ENST00000530471.1:c.471C>G	ENSP00000432669.1:p.Ala157=
NM_001145265.1:c.471C>G	NP_001138737.1:p.Ala157=
NM_001145266.1:c.471C>G	NP_001138738.1:p.Ala157=
NM_018389.4:c.510C>G , LRG_107t1:c.510C>G	NP_060859.4:p.Ala170=
XM_011520203.1:c.510C>G	XP_011518505.1:p.Ala170=
XM_011520203.3:c.510C>G	XP_011518505.1:p.Ala170=
NM_001145265.2:c.471C>G	NP_001138737.1:p.Ala157=
NM_018389.5:c.510C>G MANE Select	NP_060859.4:p.Ala170=