Canonical Allele Identifier: CA2217073305
Community Standard Title: NM_003041.4(SLC5A2):c.1435C= (p.Arg479=)
Gene: SLC5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31489034C= , CM000678.2:g.31489034C= GRCh38
NC_000016.9:g.31500355C= , CM000678.1:g.31500355C= GRCh37
NC_000016.8:g.31407856C= NCBI36
NG_012892.1:g.10917C=
NG_033149.1:g.24386G=

Transcript Alleles

HGVS Amino-acid Change
NM_003041.4:c.1435C= MANE Select NP_003032.1:p.Arg479=
ENST00000330498.4:c.1435C= MANE Select ENSP00000327943.3:p.Arg479=
NM_003041.3:c.1435C= NP_003032.1:p.Arg479=
NR_130783.1:n.1149-89C=
NR_130783.2:n.1144-89C=
ENST00000330498.3:c.1435C= ENSP00000327943.3:p.Arg479=
ENST00000419665.6:c.1130-89C= ENSP00000410601.2:n.1130-89C=
ENST00000568188.1:n.806C=
ENST00000568891.1:n.282-89C=
XM_006721072.2:c.1456C= XP_006721135.2:p.Arg486=
XM_006721072.4:c.1456C= XP_006721135.2:p.Arg486=
XM_006721073.2:c.1302-89C= XP_006721136.2:n.1302-89C=
XM_024450402.1:c.1151-89C= XP_024306170.1:n.1151-89C=