Canonical Allele Identifier: CA2575712745
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45261978A>G , CM000677.2:g.45261978A>G GRCh38
NC_000015.9:g.45554176A>G , CM000677.1:g.45554176A>G GRCh37
NC_000015.8:g.43341468A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000347644.8:c.171-37A>G (SLC28A2) MANE Select ENSP00000315006.4:n.171-37A>G
ENST00000347644.7:c.171-37A>G (SLC28A2) ENSP00000315006.4:n.171-37A>G
ENST00000560438.5:c.135-37A>G (SLC28A2) ENSP00000454074.1:n.135-37A>G
NM_004212.3:c.171-37A>G (SLC28A2) NP_004203.2:n.171-37A>G
NR_120335.1:n.27-5980T>C (SLC28A2-AS1)
XM_011522198.1:c.171-37A>G (SLC28A2) XP_011520500.1:n.171-37A>G
XM_011522199.1:c.171-37A>G (SLC28A2) XP_011520501.1:n.171-37A>G
XM_011522200.1:c.171-37A>G (SLC28A2) XP_011520502.1:n.171-37A>G
XM_011522201.1:c.171-37A>G (SLC28A2) XP_011520503.1:n.171-37A>G
XM_011522198.2:c.171-37A>G (SLC28A2) XP_011520500.1:n.171-37A>G
XM_011522200.2:c.171-37A>G (SLC28A2) XP_011520502.1:n.171-37A>G
XM_011522201.2:c.171-37A>G (SLC28A2) XP_011520503.1:n.171-37A>G
NM_004212.4:c.171-37A>G (SLC28A2) MANE Select NP_004203.2:n.171-37A>G
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