Canonical Allele Identifier: CA2542865693

Gene: SLC28A2 SLC28A2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262104del , CM000677.2:g.45262104del	GRCh38
NC_000015.9:g.45554302del , CM000677.1:g.45554302del	GRCh37
NC_000015.8:g.43341594del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.260del (SLC28A2) MANE Select	ENSP00000315006.4:p.Leu87TrpfsTer13
ENST00000347644.7:c.260del (SLC28A2)	ENSP00000315006.4:p.Leu87TrpfsTer13
ENST00000560438.5:c.224del (SLC28A2)	ENSP00000454074.1:p.Leu75TrpfsTer13
NM_004212.3:c.260del (SLC28A2)	NP_004203.2:p.Leu87TrpfsTer13
NR_120335.1:n.27-6104del (SLC28A2-AS1)
XM_011522198.1:c.260del (SLC28A2)	XP_011520500.1:p.Leu87TrpfsTer13
XM_011522199.1:c.260del (SLC28A2)	XP_011520501.1:p.Leu87TrpfsTer13
XM_011522200.1:c.260del (SLC28A2)	XP_011520502.1:p.Leu87TrpfsTer13
XM_011522201.1:c.260del (SLC28A2)	XP_011520503.1:p.Leu87TrpfsTer13
XM_011522198.2:c.260del (SLC28A2)	XP_011520500.1:p.Leu87TrpfsTer13
XM_011522200.2:c.260del (SLC28A2)	XP_011520502.1:p.Leu87TrpfsTer13
XM_011522201.2:c.260del (SLC28A2)	XP_011520503.1:p.Leu87TrpfsTer13
NM_004212.4:c.260del (SLC28A2) MANE Select	NP_004203.2:p.Leu87TrpfsTer13