Canonical Allele Identifier: CA392246597
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45262067A>C , CM000677.2:g.45262067A>C GRCh38
NC_000015.9:g.45554265A>C , CM000677.1:g.45554265A>C GRCh37
NC_000015.8:g.43341557A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000347644.8:c.223A>C (SLC28A2) MANE Select ENSP00000315006.4:p.Ser75Arg
ENST00000347644.7:c.223A>C (SLC28A2) ENSP00000315006.4:p.Ser75Arg
ENST00000560438.5:c.187A>C (SLC28A2) ENSP00000454074.1:p.Ser63Arg
NM_004212.3:c.223A>C (SLC28A2) NP_004203.2:p.Ser75Arg
NR_120335.1:n.27-6069T>G (SLC28A2-AS1)
XM_011522198.1:c.223A>C (SLC28A2) XP_011520500.1:p.Ser75Arg
XM_011522199.1:c.223A>C (SLC28A2) XP_011520501.1:p.Ser75Arg
XM_011522200.1:c.223A>C (SLC28A2) XP_011520502.1:p.Ser75Arg
XM_011522201.1:c.223A>C (SLC28A2) XP_011520503.1:p.Ser75Arg
XM_011522198.2:c.223A>C (SLC28A2) XP_011520500.1:p.Ser75Arg
XM_011522200.2:c.223A>C (SLC28A2) XP_011520502.1:p.Ser75Arg
XM_011522201.2:c.223A>C (SLC28A2) XP_011520503.1:p.Ser75Arg
NM_004212.4:c.223A>C (SLC28A2) MANE Select NP_004203.2:p.Ser75Arg