Canonical Allele Identifier: CA2581373805
Community Standard Title: NM_000453.3(SLC5A5):c.*226T>G
Gene: SLC5A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17894103T>G , CM000681.2:g.17894103T>G GRCh38
NC_000019.9:g.18004912T>G , CM000681.1:g.18004912T>G GRCh37
NC_000019.8:g.17865912T>G NCBI36
NG_012930.1:g.27131T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000453.3:c.*226T>G MANE Select NP_000444.1:n.*226T>G
ENST00000222248.4:c.*226T>G MANE Select ENSP00000222248.2:n.*226T>G
NM_000453.2:c.*226T>G NP_000444.1:n.*226T>G
ENST00000222248.3:c.*226T>G ENSP00000222248.2:n.*226T>G
XM_011528192.1:c.*226T>G XP_011526494.1:n.*226T>G
XM_011528192.2:c.*226T>G XP_011526494.1:n.*226T>G
XM_011528193.1:c.*226T>G XP_011526495.1:n.*226T>G
XM_011528193.3:c.*226T>G XP_011526495.1:n.*226T>G
XM_011528194.1:c.*226T>G XP_011526496.1:n.*226T>G
XM_011528194.3:c.*226T>G XP_011526496.1:n.*226T>G
XM_017027158.1:c.*226T>G XP_016882647.1:n.*226T>G