Canonical Allele Identifier: CA1583124891
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751173715
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340352_132340359dup , CM000667.2:g.132340352_132340359dup GRCh38
NC_000005.9:g.131676045_131676052dup , CM000667.1:g.131676045_131676052dup GRCh37
NC_000005.8:g.131703944_131703951dup NCBI36
NG_012129.1:g.50901_50908dup
NG_012129.2:g.50901_50908dup

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1445-213_1445-206dup (SLC22A4) MANE Select ENSP00000200652.3:n.1445-213_1445-206dup
ENST00000200652.3:c.1445-213_1445-206dup (SLC22A4) ENSP00000200652.3:n.1445-213_1445-206dup
NM_003059.2:c.1445-213_1445-206dup (SLC22A4) NP_003050.2:n.1445-213_1445-206dup
NR_110997.1:n.561-5433_561-5426dup (MIR3936HG)
XM_006714675.2:c.917-213_917-206dup (SLC22A4) XP_006714738.1:n.917-213_917-206dup
XM_011543589.1:c.1169-213_1169-206dup (SLC22A4) XP_011541891.1:n.1169-213_1169-206dup
XM_006714675.4:c.917-213_917-206dup (SLC22A4) XP_006714738.1:n.917-213_917-206dup
XM_011543589.2:c.1169-213_1169-206dup (SLC22A4) XP_011541891.1:n.1169-213_1169-206dup
XM_017009776.1:c.917-213_917-206dup (SLC22A4) XP_016865265.1:n.917-213_917-206dup
NM_003059.3:c.1445-213_1445-206dup (SLC22A4) MANE Select NP_003050.2:n.1445-213_1445-206dup
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