Canonical Allele Identifier: CA3403427

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs751767313
• ExAC: 5:131649278 CAT / C
• gnomAD v2: 5-131649278-CAT-C
• gnomAD v4: 5-132313585-CAT-C
• MyVariant Identifiers: chr5:g.131649279_131649280del (hg19) ; chr5:g.132313586_132313587del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313586_132313587del , CM000667.2:g.132313586_132313587del	GRCh38
NC_000005.9:g.131649279_131649280del , CM000667.1:g.131649279_131649280del	GRCh37
NC_000005.8:g.131677178_131677179del	NCBI36
NG_012129.1:g.24135_24136del
NG_012129.2:g.24135_24136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-28_498-27del (SLC22A4) MANE Select	ENSP00000200652.3:n.498-28_498-27del
ENST00000200652.3:c.498-28_498-27del (SLC22A4)	ENSP00000200652.3:n.498-28_498-27del
ENST00000491257.1:n.302-28_302-27del (SLC22A4)
NM_003059.2:c.498-28_498-27del (SLC22A4)	NP_003050.2:n.498-28_498-27del
NR_110997.1:n.825-1334_825-1333del (MIR3936HG)
XM_006714675.2:c.-31-28_-31-27del (SLC22A4)	XP_006714738.1:n.-31-28_-31-27del
XM_011543589.1:c.394-28_394-27del (SLC22A4)	XP_011541891.1:n.394-28_394-27del
XM_006714675.4:c.-31-28_-31-27del (SLC22A4)	XP_006714738.1:n.-31-28_-31-27del
XM_011543589.2:c.394-28_394-27del (SLC22A4)	XP_011541891.1:n.394-28_394-27del
XM_017009776.1:c.-31-28_-31-27del (SLC22A4)	XP_016865265.1:n.-31-28_-31-27del
NM_003059.3:c.498-28_498-27del (SLC22A4) MANE Select	NP_003050.2:n.498-28_498-27del