Canonical Allele Identifier: CA562764488

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1561550067
• gnomAD v2: 5-131676234-GT-G
• gnomAD v4: 5-132340541-GT-G
• MyVariant Identifiers: chr5:g.131676235del (hg19) ; chr5:g.132340542del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340543del , CM000667.2:g.132340543del	GRCh38
NC_000005.9:g.131676236del , CM000667.1:g.131676236del	GRCh37
NC_000005.8:g.131704135del	NCBI36
NG_012129.1:g.51092del
NG_012129.2:g.51092del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1445-22del (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-22del
ENST00000200652.3:c.1445-22del (SLC22A4)	ENSP00000200652.3:n.1445-22del
NM_003059.2:c.1445-22del (SLC22A4)	NP_003050.2:n.1445-22del
NR_110997.1:n.561-5616del (MIR3936HG)
XM_006714675.2:c.917-22del (SLC22A4)	XP_006714738.1:n.917-22del
XM_011543589.1:c.1169-22del (SLC22A4)	XP_011541891.1:n.1169-22del
XM_006714675.4:c.917-22del (SLC22A4)	XP_006714738.1:n.917-22del
XM_011543589.2:c.1169-22del (SLC22A4)	XP_011541891.1:n.1169-22del
XM_017009776.1:c.917-22del (SLC22A4)	XP_016865265.1:n.917-22del
NM_003059.3:c.1445-22del (SLC22A4) MANE Select	NP_003050.2:n.1445-22del