Canonical Allele Identifier: CA360804016

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649399C>A (hg19) ; chr5:g.132313706C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313706C>A , CM000667.2:g.132313706C>A	GRCh38
NC_000005.9:g.131649399C>A , CM000667.1:g.131649399C>A	GRCh37
NC_000005.8:g.131677298C>A	NCBI36
NG_012129.1:g.24255C>A
NG_012129.2:g.24255C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.590C>A (SLC22A4) MANE Select	ENSP00000200652.3:p.Thr197Asn
ENST00000200652.3:c.590C>A (SLC22A4)	ENSP00000200652.3:p.Thr197Asn
ENST00000491257.1:n.394C>A (SLC22A4)
NM_003059.2:c.590C>A (SLC22A4)	NP_003050.2:p.Thr197Asn
NR_110997.1:n.825-1453G>T (MIR3936HG)
XM_006714675.2:c.62C>A (SLC22A4)	XP_006714738.1:p.Thr21Asn
XM_011543589.1:c.486C>A (SLC22A4)	XP_011541891.1:p.His162Gln
XM_006714675.4:c.62C>A (SLC22A4)	XP_006714738.1:p.Thr21Asn
XM_011543589.2:c.486C>A (SLC22A4)	XP_011541891.1:p.His162Gln
XM_017009776.1:c.62C>A (SLC22A4)	XP_016865265.1:p.Thr21Asn
NM_003059.3:c.590C>A (SLC22A4) MANE Select	NP_003050.2:p.Thr197Asn