Canonical Allele Identifier: CA2628262028

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• gnomAD v4: 15-45253280-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45253283_45253284del , CM000677.2:g.45253283_45253284del	GRCh38
NC_000015.9:g.45545481_45545482del , CM000677.1:g.45545481_45545482del	GRCh37
NC_000015.8:g.43332773_43332774del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.68_69del (SLC28A2) MANE Select	ENSP00000315006.4:p.Gly23AlafsTer11
ENST00000347644.7:c.68_69del (SLC28A2)	ENSP00000315006.4:p.Gly23AlafsTer11
ENST00000560438.5:c.46-149_46-148del (SLC28A2)	ENSP00000454074.1:n.46-149_46-148del
NM_004212.3:c.68_69del (SLC28A2)	NP_004203.2:p.Gly23AlafsTer11
NR_120335.1:n.180+584_180+585del (SLC28A2-AS1)
XM_011522198.1:c.68_69del (SLC28A2)	XP_011520500.1:p.Gly23AlafsTer11
XM_011522199.1:c.68_69del (SLC28A2)	XP_011520501.1:p.Gly23AlafsTer11
XM_011522200.1:c.68_69del (SLC28A2)	XP_011520502.1:p.Gly23AlafsTer11
XM_011522201.1:c.68_69del (SLC28A2)	XP_011520503.1:p.Gly23AlafsTer11
XM_011522198.2:c.68_69del (SLC28A2)	XP_011520500.1:p.Gly23AlafsTer11
XM_011522200.2:c.68_69del (SLC28A2)	XP_011520502.1:p.Gly23AlafsTer11
XM_011522201.2:c.68_69del (SLC28A2)	XP_011520503.1:p.Gly23AlafsTer11
NM_004212.4:c.68_69del (SLC28A2) MANE Select	NP_004203.2:p.Gly23AlafsTer11