Canonical Allele Identifier: CA2583492580

Gene: SLC5A5

Linked Data

• gnomAD v4: 19-17894018-C-CATAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17894018_17894019insATAGGG , CM000681.2:g.17894018_17894019insATAGGG	GRCh38
NC_000019.9:g.18004827_18004828insATAGGG , CM000681.1:g.18004827_18004828insATAGGG	GRCh37
NC_000019.8:g.17865827_17865828insATAGGG	NCBI36
NG_012930.1:g.27046_27047insATAGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000222248.4:c.*141_*142insATAGGG MANE Select	ENSP00000222248.2:n.*141_*142insATAGGG
ENST00000222248.3:c.*141_*142insATAGGG	ENSP00000222248.2:n.*141_*142insATAGGG
NM_000453.2:c.*141_*142insATAGGG	NP_000444.1:n.*141_*142insATAGGG
XM_011528192.1:c.*141_*142insATAGGG	XP_011526494.1:n.*141_*142insATAGGG
XM_011528193.1:c.*141_*142insATAGGG	XP_011526495.1:n.*141_*142insATAGGG
XM_011528194.1:c.*141_*142insATAGGG	XP_011526496.1:n.*141_*142insATAGGG
XM_011528192.2:c.*141_*142insATAGGG	XP_011526494.1:n.*141_*142insATAGGG
XM_011528193.3:c.*141_*142insATAGGG	XP_011526495.1:n.*141_*142insATAGGG
XM_011528194.3:c.*141_*142insATAGGG	XP_011526496.1:n.*141_*142insATAGGG
XM_017027158.1:c.*141_*142insATAGGG	XP_016882647.1:n.*141_*142insATAGGG
NM_000453.3:c.*141_*142insATAGGG MANE Select	NP_000444.1:n.*141_*142insATAGGG