Canonical Allele Identifier: CA2174015671

Gene: SLC28A2 SLC28A2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262003G= , CM000677.2:g.45262003G=	GRCh38
NC_000015.9:g.45554201G= , CM000677.1:g.45554201G=	GRCh37
NC_000015.8:g.43341493G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.171-12G= (SLC28A2) MANE Select	ENSP00000315006.4:n.171-12G=
ENST00000347644.7:c.171-12G= (SLC28A2)	ENSP00000315006.4:n.171-12G=
ENST00000560438.5:c.135-12G= (SLC28A2)	ENSP00000454074.1:n.135-12G=
NM_004212.3:c.171-12G= (SLC28A2)	NP_004203.2:n.171-12G=
NR_120335.1:n.27-6005C= (SLC28A2-AS1)
XM_011522198.1:c.171-12G= (SLC28A2)	XP_011520500.1:n.171-12G=
XM_011522199.1:c.171-12G= (SLC28A2)	XP_011520501.1:n.171-12G=
XM_011522200.1:c.171-12G= (SLC28A2)	XP_011520502.1:n.171-12G=
XM_011522201.1:c.171-12G= (SLC28A2)	XP_011520503.1:n.171-12G=
XM_011522198.2:c.171-12G= (SLC28A2)	XP_011520500.1:n.171-12G=
XM_011522200.2:c.171-12G= (SLC28A2)	XP_011520502.1:n.171-12G=
XM_011522201.2:c.171-12G= (SLC28A2)	XP_011520503.1:n.171-12G=
NM_004212.4:c.171-12G= (SLC28A2) MANE Select	NP_004203.2:n.171-12G=