Canonical Allele Identifier: CA2675193154
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

gnomAD v4: 5-132335684-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132335688dup , CM000667.2:g.132335688dup GRCh38
NC_000005.9:g.131671381dup , CM000667.1:g.131671381dup GRCh37
NC_000005.8:g.131699280dup NCBI36
NG_012129.1:g.46237dup
NG_012129.2:g.46237dup

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1262-130dup (SLC22A4) MANE Select ENSP00000200652.3:n.1262-130dup
ENST00000200652.3:c.1262-130dup (SLC22A4) ENSP00000200652.3:n.1262-130dup
NM_003059.2:c.1262-130dup (SLC22A4) NP_003050.2:n.1262-130dup
NR_110997.1:n.561-759dup (MIR3936HG)
XM_006714675.2:c.734-130dup (SLC22A4) XP_006714738.1:n.734-130dup
XM_011543589.1:c.986-130dup (SLC22A4) XP_011541891.1:n.986-130dup
XM_006714675.4:c.734-130dup (SLC22A4) XP_006714738.1:n.734-130dup
XM_011543589.2:c.986-130dup (SLC22A4) XP_011541891.1:n.986-130dup
XM_017009776.1:c.734-130dup (SLC22A4) XP_016865265.1:n.734-130dup
NM_003059.3:c.1262-130dup (SLC22A4) MANE Select NP_003050.2:n.1262-130dup
Search 100 bp 5'
Search 100 bp 3'