Canonical Allele Identifier: CA346163484
Gene: SLC5A6 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27201768G>T , CM000664.2:g.27201768G>T GRCh38
NC_000002.11:g.27424636G>T , CM000664.1:g.27424636G>T GRCh37
NC_000002.10:g.27278140G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310574.8:c.1442C>A MANE Select ENSP00000310208.3:p.Ser481Tyr
ENST00000310574.7:c.1442C>A ENSP00000310208.3:p.Ser481Tyr
ENST00000408041.5:c.1442C>A ENSP00000384853.1:p.Ser481Tyr
ENST00000461319.5:n.380C>A
ENST00000461757.1:n.544C>A
ENST00000481751.5:n.471C>A
ENST00000488743.6:n.2128C>A
ENST00000492069.5:n.649C>A
NM_021095.2:c.1442C>A NP_066918.2:p.Ser481Tyr
NR_028323.1:n.2289C>A
XM_006712128.1:c.1442C>A XP_006712191.1:p.Ser481Tyr
XM_006712129.1:c.1442C>A XP_006712192.1:p.Ser481Tyr
XM_006712130.1:c.1442C>A XP_006712193.1:p.Ser481Tyr
XM_011533144.1:c.1442C>A XP_011531446.1:p.Ser481Tyr
XM_011533145.1:c.1442C>A XP_011531447.1:p.Ser481Tyr
XM_011533146.1:c.773C>A XP_011531448.1:p.Ser258Tyr
XR_939737.1:n.2289C>A
XM_006712128.2:c.1442C>A XP_006712191.1:p.Ser481Tyr
XM_011533146.3:c.773C>A XP_011531448.1:p.Ser258Tyr
XM_017005216.1:c.815C>A XP_016860705.1:p.Ser272Tyr
XM_024453206.1:c.1442C>A XP_024308974.1:p.Ser481Tyr
XM_024453207.1:c.1442C>A XP_024308975.1:p.Ser481Tyr
XR_001739022.1:n.1738C>A
XR_001739023.1:n.1668C>A
XR_001739024.2:n.1735C>A
XR_001739025.2:n.1674C>A
XR_002959356.1:n.1972C>A
XR_002959357.1:n.1907C>A
XR_002959358.1:n.1907C>A
NM_021095.3:c.1442C>A NP_066918.2:p.Ser481Tyr
NM_021095.4:c.1442C>A MANE Select NP_066918.2:p.Ser481Tyr
NR_028323.2:n.2250C>A