Canonical Allele Identifier: CA2217073047

Gene: SLC5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31488944G= , CM000678.2:g.31488944G=	GRCh38
NC_000016.9:g.31500265G= , CM000678.1:g.31500265G=	GRCh37
NC_000016.8:g.31407766G=	NCBI36
NG_012892.1:g.10827G=
NG_033149.1:g.24476C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330498.4:c.1345G= MANE Select	ENSP00000327943.3:p.Gly449=
ENST00000330498.3:c.1345G=	ENSP00000327943.3:p.Gly449=
ENST00000419665.6:c.1130-179G=	ENSP00000410601.2:n.1130-179G=
ENST00000568188.1:n.716G=
ENST00000568891.1:n.282-179G=
NM_003041.3:c.1345G=	NP_003032.1:p.Gly449=
NR_130783.1:n.1149-179G=
XM_006721072.2:c.1366G=	XP_006721135.2:p.Gly456=
XM_006721073.2:c.1301+172G=	XP_006721136.2:n.1301+172G=
XM_006721072.4:c.1366G=	XP_006721135.2:p.Gly456=
XM_024450402.1:c.1151-179G=	XP_024306170.1:n.1151-179G=
NM_003041.4:c.1345G= MANE Select	NP_003032.1:p.Gly449=
NR_130783.2:n.1144-179G=