Canonical Allele Identifier: CA3217521999

Gene: SLC5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31486201A= , CM000678.2:g.31486201A=	GRCh38
NC_000016.9:g.31497522A= , CM000678.1:g.31497522A=	GRCh37
NC_000016.8:g.31405023A=	NCBI36
NG_012892.1:g.8084A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330498.4:c.500A= MANE Select	ENSP00000327943.3:p.Gln167=
ENST00000330498.3:c.500A=	ENSP00000327943.3:p.Gln167=
ENST00000419665.6:c.500A=	ENSP00000410601.2:p.Gln167=
ENST00000565446.1:n.374A=
ENST00000569576.5:c.371A=	ENSP00000455143.1:p.Gln124=
NM_003041.3:c.500A=	NP_003032.1:p.Gln167=
NR_130783.1:n.519A=
XM_006721072.2:c.521A=	XP_006721135.2:p.Gln174=
XM_006721073.2:c.521A=	XP_006721136.2:p.Gln174=
XM_006721072.4:c.521A=	XP_006721135.2:p.Gln174=
XM_024450402.1:c.521A=	XP_024306170.1:p.Gln174=
NM_003041.4:c.500A= MANE Select	NP_003032.1:p.Gln167=
NR_130783.2:n.514A=