Canonical Allele Identifier: CA2174011538

Gene: SLC28A2 SLC28A2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45253289A= , CM000677.2:g.45253289A=	GRCh38
NC_000015.9:g.45545487A= , CM000677.1:g.45545487A=	GRCh37
NC_000015.8:g.43332779A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.74A= (SLC28A2) MANE Select	ENSP00000315006.4:p.Glu25=
ENST00000347644.7:c.74A= (SLC28A2)	ENSP00000315006.4:p.Glu25=
ENST00000560438.5:c.46-143A= (SLC28A2)	ENSP00000454074.1:n.46-143A=
NM_004212.3:c.74A= (SLC28A2)	NP_004203.2:p.Glu25=
NR_120335.1:n.180+577T= (SLC28A2-AS1)
XM_011522198.1:c.74A= (SLC28A2)	XP_011520500.1:p.Glu25=
XM_011522199.1:c.74A= (SLC28A2)	XP_011520501.1:p.Glu25=
XM_011522200.1:c.74A= (SLC28A2)	XP_011520502.1:p.Glu25=
XM_011522201.1:c.74A= (SLC28A2)	XP_011520503.1:p.Glu25=
XM_011522198.2:c.74A= (SLC28A2)	XP_011520500.1:p.Glu25=
XM_011522200.2:c.74A= (SLC28A2)	XP_011520502.1:p.Glu25=
XM_011522201.2:c.74A= (SLC28A2)	XP_011520503.1:p.Glu25=
NM_004212.4:c.74A= (SLC28A2) MANE Select	NP_004203.2:p.Glu25=