Canonical Allele Identifier: CA783886584

Gene: SLC5A5

Linked Data

• dbSNP Id: rs1165626278
• MyVariant Identifiers: chr19:g.18001850A>G (hg19) ; chr19:g.17891041A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17891041A>G , CM000681.2:g.17891041A>G	GRCh38
NC_000019.9:g.18001850A>G , CM000681.1:g.18001850A>G	GRCh37
NC_000019.8:g.17862850A>G	NCBI36
NG_012930.1:g.24069A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222248.4:c.1767+40A>G MANE Select	ENSP00000222248.2:n.1767+40A>G
ENST00000222248.3:c.1767+40A>G	ENSP00000222248.2:n.1767+40A>G
NM_000453.2:c.1767+40A>G	NP_000444.1:n.1767+40A>G
XM_011528192.1:c.1800+40A>G	XP_011526494.1:n.1800+40A>G
XM_011528193.1:c.1533+40A>G	XP_011526495.1:n.1533+40A>G
XM_011528194.1:c.1434+40A>G	XP_011526496.1:n.1434+40A>G
XM_011528192.2:c.1800+40A>G	XP_011526494.1:n.1800+40A>G
XM_011528193.3:c.1533+40A>G	XP_011526495.1:n.1533+40A>G
XM_011528194.3:c.1434+40A>G	XP_011526496.1:n.1434+40A>G
XM_017027158.1:c.1500+40A>G	XP_016882647.1:n.1500+40A>G
NM_000453.3:c.1767+40A>G MANE Select	NP_000444.1:n.1767+40A>G