Canonical Allele Identifier: CA395755459

Gene: SLC5A2

Linked Data

• MyVariant Identifiers: chr16:g.31500445G>C (hg19) ; chr16:g.31489124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31489124G>C , CM000678.2:g.31489124G>C	GRCh38
NC_000016.9:g.31500445G>C , CM000678.1:g.31500445G>C	GRCh37
NC_000016.8:g.31407946G>C	NCBI36
NG_012892.1:g.11007G>C
NG_033149.1:g.24296C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330498.4:c.1451G>C MANE Select	ENSP00000327943.3:p.Gly484Ala
ENST00000330498.3:c.1451G>C	ENSP00000327943.3:p.Gly484Ala
ENST00000419665.6:c.1131G>C	ENSP00000410601.2:p.Gly377=
ENST00000568188.1:n.822G>C
ENST00000568891.1:n.283G>C
NM_003041.3:c.1451G>C	NP_003032.1:p.Gly484Ala
NR_130783.1:n.1150G>C
XM_006721072.2:c.1472G>C	XP_006721135.2:p.Gly491Ala
XM_006721073.2:c.1303G>C	XP_006721136.2:p.Ala435Pro
XM_006721072.4:c.1472G>C	XP_006721135.2:p.Gly491Ala
XM_024450402.1:c.1152G>C	XP_024306170.1:p.Gly384=
NM_003041.4:c.1451G>C MANE Select	NP_003032.1:p.Gly484Ala
NR_130783.2:n.1145G>C