Canonical Allele Identifier: CA395755403

Gene: SLC5A2

Linked Data

• MyVariant Identifiers: chr16:g.31500367C>T (hg19) ; chr16:g.31489046C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31489046C>T , CM000678.2:g.31489046C>T	GRCh38
NC_000016.9:g.31500367C>T , CM000678.1:g.31500367C>T	GRCh37
NC_000016.8:g.31407868C>T	NCBI36
NG_012892.1:g.10929C>T
NG_033149.1:g.24374G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330498.4:c.1447C>T MANE Select	ENSP00000327943.3:p.Gln483Ter
ENST00000330498.3:c.1447C>T	ENSP00000327943.3:p.Gln483Ter
ENST00000419665.6:c.1130-77C>T	ENSP00000410601.2:n.1130-77C>T
ENST00000568188.1:n.818C>T
ENST00000568891.1:n.282-77C>T
NM_003041.3:c.1447C>T	NP_003032.1:p.Gln483Ter
NR_130783.1:n.1149-77C>T
XM_006721072.2:c.1468C>T	XP_006721135.2:p.Gln490Ter
XM_006721073.2:c.1302-77C>T	XP_006721136.2:n.1302-77C>T
XM_006721072.4:c.1468C>T	XP_006721135.2:p.Gln490Ter
XM_024450402.1:c.1151-77C>T	XP_024306170.1:n.1151-77C>T
NM_003041.4:c.1447C>T MANE Select	NP_003032.1:p.Gln483Ter
NR_130783.2:n.1144-77C>T