Canonical Allele Identifier: CA7542136

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• dbSNP Id: rs774274812
• ExAC: 15:45554334 AAACACAGTT / A
• gnomAD v2: 15-45554334-AAACACAGTT-A
• gnomAD v3: 15-45262136-AAACACAGTT-A
• gnomAD v4: 15-45262136-AAACACAGTT-A
• MyVariant Identifiers: chr15:g.45554335_45554343del (hg19) ; chr15:g.45262137_45262145del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262138_45262146del , CM000677.2:g.45262138_45262146del	GRCh38
NC_000015.9:g.45554336_45554344del , CM000677.1:g.45554336_45554344del	GRCh37
NC_000015.8:g.43341628_43341636del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.262+32_262+40del (SLC28A2) MANE Select	ENSP00000315006.4:n.262+32_262+40del
ENST00000347644.7:c.262+32_262+40del (SLC28A2)	ENSP00000315006.4:n.262+32_262+40del
ENST00000560438.5:c.226+32_226+40del (SLC28A2)	ENSP00000454074.1:n.226+32_226+40del
NM_004212.3:c.262+32_262+40del (SLC28A2)	NP_004203.2:n.262+32_262+40del
NR_120335.1:n.27-6147_27-6139del (SLC28A2-AS1)
XM_011522198.1:c.262+32_262+40del (SLC28A2)	XP_011520500.1:n.262+32_262+40del
XM_011522199.1:c.262+32_262+40del (SLC28A2)	XP_011520501.1:n.262+32_262+40del
XM_011522200.1:c.262+32_262+40del (SLC28A2)	XP_011520502.1:n.262+32_262+40del
XM_011522201.1:c.262+32_262+40del (SLC28A2)	XP_011520503.1:n.262+32_262+40del
XM_011522198.2:c.262+32_262+40del (SLC28A2)	XP_011520500.1:n.262+32_262+40del
XM_011522200.2:c.262+32_262+40del (SLC28A2)	XP_011520502.1:n.262+32_262+40del
XM_011522201.2:c.262+32_262+40del (SLC28A2)	XP_011520503.1:n.262+32_262+40del
NM_004212.4:c.262+32_262+40del (SLC28A2) MANE Select	NP_004203.2:n.262+32_262+40del