Canonical Allele Identifier: CA803997997

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1407519927
• gnomAD v3: 5-132313835-T-TCATTGGGC
• gnomAD v4: 5-132313835-T-TCATTGGGC
• MyVariant Identifiers: chr5:g.131649528_131649529insCATTGGGC (hg19) ; chr5:g.132313835_132313836insCATTGGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313844_132313851dup , CM000667.2:g.132313844_132313851dup	GRCh38
NC_000005.9:g.131649537_131649544dup , CM000667.1:g.131649537_131649544dup	GRCh37
NC_000005.8:g.131677436_131677443dup	NCBI36
NG_012129.1:g.24393_24400dup
NG_012129.2:g.24393_24400dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+76_652+83dup (SLC22A4) MANE Select	ENSP00000200652.3:n.652+76_652+83dup
ENST00000200652.3:c.652+76_652+83dup (SLC22A4)	ENSP00000200652.3:n.652+76_652+83dup
ENST00000491257.1:n.456+76_456+83dup (SLC22A4)
NM_003059.2:c.652+76_652+83dup (SLC22A4)	NP_003050.2:n.652+76_652+83dup
NR_110997.1:n.825-1590_825-1583dup (MIR3936HG)
XM_006714675.2:c.124+76_124+83dup (SLC22A4)	XP_006714738.1:n.124+76_124+83dup
XM_011543589.1:c.548+76_548+83dup (SLC22A4)	XP_011541891.1:n.548+76_548+83dup
XM_006714675.4:c.124+76_124+83dup (SLC22A4)	XP_006714738.1:n.124+76_124+83dup
XM_011543589.2:c.548+76_548+83dup (SLC22A4)	XP_011541891.1:n.548+76_548+83dup
XM_017009776.1:c.124+76_124+83dup (SLC22A4)	XP_016865265.1:n.124+76_124+83dup
NM_003059.3:c.652+76_652+83dup (SLC22A4) MANE Select	NP_003050.2:n.652+76_652+83dup