Canonical Allele Identifier: CA392246602

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• MyVariant Identifiers: chr15:g.45554268T>A (hg19) ; chr15:g.45262070T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262070T>A , CM000677.2:g.45262070T>A	GRCh38
NC_000015.9:g.45554268T>A , CM000677.1:g.45554268T>A	GRCh37
NC_000015.8:g.43341560T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.226T>A (SLC28A2) MANE Select	ENSP00000315006.4:p.Leu76Met
ENST00000347644.7:c.226T>A (SLC28A2)	ENSP00000315006.4:p.Leu76Met
ENST00000560438.5:c.190T>A (SLC28A2)	ENSP00000454074.1:p.Leu64Met
NM_004212.3:c.226T>A (SLC28A2)	NP_004203.2:p.Leu76Met
NR_120335.1:n.27-6072A>T (SLC28A2-AS1)
XM_011522198.1:c.226T>A (SLC28A2)	XP_011520500.1:p.Leu76Met
XM_011522199.1:c.226T>A (SLC28A2)	XP_011520501.1:p.Leu76Met
XM_011522200.1:c.226T>A (SLC28A2)	XP_011520502.1:p.Leu76Met
XM_011522201.1:c.226T>A (SLC28A2)	XP_011520503.1:p.Leu76Met
XM_011522198.2:c.226T>A (SLC28A2)	XP_011520500.1:p.Leu76Met
XM_011522200.2:c.226T>A (SLC28A2)	XP_011520502.1:p.Leu76Met
XM_011522201.2:c.226T>A (SLC28A2)	XP_011520503.1:p.Leu76Met
NM_004212.4:c.226T>A (SLC28A2) MANE Select	NP_004203.2:p.Leu76Met