Canonical Allele Identifier: CA2578401724

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132313868-TTGGATATATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313871_132313880del , CM000667.2:g.132313871_132313880del	GRCh38
NC_000005.9:g.131649564_131649573del , CM000667.1:g.131649564_131649573del	GRCh37
NC_000005.8:g.131677463_131677472del	NCBI36
NG_012129.1:g.24420_24429del
NG_012129.2:g.24420_24429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+103_652+112del (SLC22A4) MANE Select	ENSP00000200652.3:n.652+103_652+112del
ENST00000200652.3:c.652+103_652+112del (SLC22A4)	ENSP00000200652.3:n.652+103_652+112del
ENST00000491257.1:n.456+103_456+112del (SLC22A4)
NM_003059.2:c.652+103_652+112del (SLC22A4)	NP_003050.2:n.652+103_652+112del
NR_110997.1:n.825-1625_825-1616del (MIR3936HG)
XM_006714675.2:c.124+103_124+112del (SLC22A4)	XP_006714738.1:n.124+103_124+112del
XM_011543589.1:c.548+103_548+112del (SLC22A4)	XP_011541891.1:n.548+103_548+112del
XM_006714675.4:c.124+103_124+112del (SLC22A4)	XP_006714738.1:n.124+103_124+112del
XM_011543589.2:c.548+103_548+112del (SLC22A4)	XP_011541891.1:n.548+103_548+112del
XM_017009776.1:c.124+103_124+112del (SLC22A4)	XP_016865265.1:n.124+103_124+112del
NM_003059.3:c.652+103_652+112del (SLC22A4) MANE Select	NP_003050.2:n.652+103_652+112del