Canonical Allele Identifier: CA1081630890

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1750255859
• gnomAD v3: 5-132313824-GAAAGAGGA-G
• gnomAD v4: 5-132313824-GAAAGAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313827_132313834del , CM000667.2:g.132313827_132313834del	GRCh38
NC_000005.9:g.131649520_131649527del , CM000667.1:g.131649520_131649527del	GRCh37
NC_000005.8:g.131677419_131677426del	NCBI36
NG_012129.1:g.24376_24383del
NG_012129.2:g.24376_24383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+59_652+66del (SLC22A4) MANE Select	ENSP00000200652.3:n.652+59_652+66del
ENST00000200652.3:c.652+59_652+66del (SLC22A4)	ENSP00000200652.3:n.652+59_652+66del
ENST00000491257.1:n.456+59_456+66del (SLC22A4)
NM_003059.2:c.652+59_652+66del (SLC22A4)	NP_003050.2:n.652+59_652+66del
NR_110997.1:n.825-1579_825-1572del (MIR3936HG)
XM_006714675.2:c.124+59_124+66del (SLC22A4)	XP_006714738.1:n.124+59_124+66del
XM_011543589.1:c.548+59_548+66del (SLC22A4)	XP_011541891.1:n.548+59_548+66del
XM_006714675.4:c.124+59_124+66del (SLC22A4)	XP_006714738.1:n.124+59_124+66del
XM_011543589.2:c.548+59_548+66del (SLC22A4)	XP_011541891.1:n.548+59_548+66del
XM_017009776.1:c.124+59_124+66del (SLC22A4)	XP_016865265.1:n.124+59_124+66del
NM_003059.3:c.652+59_652+66del (SLC22A4) MANE Select	NP_003050.2:n.652+59_652+66del