Canonical Allele Identifier: CA395755205

Gene: SLC5A2

Linked Data

• gnomAD v4: 16-31488969-A-C
• MyVariant Identifiers: chr16:g.31500290A>C (hg19) ; chr16:g.31488969A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31488969A>C , CM000678.2:g.31488969A>C	GRCh38
NC_000016.9:g.31500290A>C , CM000678.1:g.31500290A>C	GRCh37
NC_000016.8:g.31407791A>C	NCBI36
NG_012892.1:g.10852A>C
NG_033149.1:g.24451T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330498.4:c.1370A>C MANE Select	ENSP00000327943.3:p.Gln457Pro
ENST00000330498.3:c.1370A>C	ENSP00000327943.3:p.Gln457Pro
ENST00000419665.6:c.1130-154A>C	ENSP00000410601.2:n.1130-154A>C
ENST00000568188.1:n.741A>C
ENST00000568891.1:n.282-154A>C
NM_003041.3:c.1370A>C	NP_003032.1:p.Gln457Pro
NR_130783.1:n.1149-154A>C
XM_006721072.2:c.1391A>C	XP_006721135.2:p.Gln464Pro
XM_006721073.2:c.1302-154A>C	XP_006721136.2:n.1302-154A>C
XM_006721072.4:c.1391A>C	XP_006721135.2:p.Gln464Pro
XM_024450402.1:c.1151-154A>C	XP_024306170.1:n.1151-154A>C
NM_003041.4:c.1370A>C MANE Select	NP_003032.1:p.Gln457Pro
NR_130783.2:n.1144-154A>C