Canonical Allele Identifier: CA2675191044

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132313520-AAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313522_132313524del , CM000667.2:g.132313522_132313524del	GRCh38
NC_000005.9:g.131649215_131649217del , CM000667.1:g.131649215_131649217del	GRCh37
NC_000005.8:g.131677114_131677116del	NCBI36
NG_012129.1:g.24071_24073del
NG_012129.2:g.24071_24073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-92_498-90del (SLC22A4) MANE Select	ENSP00000200652.3:n.498-92_498-90del
ENST00000200652.3:c.498-92_498-90del (SLC22A4)	ENSP00000200652.3:n.498-92_498-90del
ENST00000491257.1:n.302-92_302-90del (SLC22A4)
NM_003059.2:c.498-92_498-90del (SLC22A4)	NP_003050.2:n.498-92_498-90del
NR_110997.1:n.825-1270_825-1268del (MIR3936HG)
XM_006714675.2:c.-31-92_-31-90del (SLC22A4)	XP_006714738.1:n.-31-92_-31-90del
XM_011543589.1:c.394-92_394-90del (SLC22A4)	XP_011541891.1:n.394-92_394-90del
XM_006714675.4:c.-31-92_-31-90del (SLC22A4)	XP_006714738.1:n.-31-92_-31-90del
XM_011543589.2:c.394-92_394-90del (SLC22A4)	XP_011541891.1:n.394-92_394-90del
XM_017009776.1:c.-31-92_-31-90del (SLC22A4)	XP_016865265.1:n.-31-92_-31-90del
NM_003059.3:c.498-92_498-90del (SLC22A4) MANE Select	NP_003050.2:n.498-92_498-90del