Canonical Allele Identifier: CA360813379
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340667C>A , CM000667.2:g.132340667C>A GRCh38
NC_000005.9:g.131676360C>A , CM000667.1:g.131676360C>A GRCh37
NC_000005.8:g.131704259C>A NCBI36
NG_012129.1:g.51216C>A
NG_012129.2:g.51216C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.1547C>A (SLC22A4) MANE Select ENSP00000200652.3:p.Pro516Gln
ENST00000200652.3:c.1547C>A (SLC22A4) ENSP00000200652.3:p.Pro516Gln
NM_003059.2:c.1547C>A (SLC22A4) NP_003050.2:p.Pro516Gln
NR_110997.1:n.561-5741G>T (MIR3936HG)
XM_006714675.2:c.1019C>A (SLC22A4) XP_006714738.1:p.Pro340Gln
XM_011543589.1:c.1271C>A (SLC22A4) XP_011541891.1:p.Pro424Gln
XM_006714675.4:c.1019C>A (SLC22A4) XP_006714738.1:p.Pro340Gln
XM_011543589.2:c.1271C>A (SLC22A4) XP_011541891.1:p.Pro424Gln
XM_017009776.1:c.1019C>A (SLC22A4) XP_016865265.1:p.Pro340Gln
NM_003059.3:c.1547C>A (SLC22A4) MANE Select NP_003050.2:p.Pro516Gln