Canonical Allele Identifier: CA7542107
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs781669494
ExAC: 15:45554180 ATTC / A
gnomAD v2: 15-45554180-ATTC-A
gnomAD v3: 15-45261982-ATTC-A
gnomAD v4: 15-45261982-ATTC-A
MyVariant Identifiers: chr15:g.45554181_45554183del (hg19) chr15:g.45261983_45261985del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45261985_45261987del , CM000677.2:g.45261985_45261987del GRCh38
NC_000015.9:g.45554183_45554185del , CM000677.1:g.45554183_45554185del GRCh37
NC_000015.8:g.43341475_43341477del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000347644.8:c.171-30_171-28del (SLC28A2) MANE Select ENSP00000315006.4:n.171-30_171-28del
ENST00000347644.7:c.171-30_171-28del (SLC28A2) ENSP00000315006.4:n.171-30_171-28del
ENST00000560438.5:c.135-30_135-28del (SLC28A2) ENSP00000454074.1:n.135-30_135-28del
NM_004212.3:c.171-30_171-28del (SLC28A2) NP_004203.2:n.171-30_171-28del
NR_120335.1:n.27-5987_27-5985del (SLC28A2-AS1)
XM_011522198.1:c.171-30_171-28del (SLC28A2) XP_011520500.1:n.171-30_171-28del
XM_011522199.1:c.171-30_171-28del (SLC28A2) XP_011520501.1:n.171-30_171-28del
XM_011522200.1:c.171-30_171-28del (SLC28A2) XP_011520502.1:n.171-30_171-28del
XM_011522201.1:c.171-30_171-28del (SLC28A2) XP_011520503.1:n.171-30_171-28del
XM_011522198.2:c.171-30_171-28del (SLC28A2) XP_011520500.1:n.171-30_171-28del
XM_011522200.2:c.171-30_171-28del (SLC28A2) XP_011520502.1:n.171-30_171-28del
XM_011522201.2:c.171-30_171-28del (SLC28A2) XP_011520503.1:n.171-30_171-28del
NM_004212.4:c.171-30_171-28del (SLC28A2) MANE Select NP_004203.2:n.171-30_171-28del
Search 100 bp 5'
Search 100 bp 3'