Canonical Allele Identifier: CA1583118360

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313652T= , CM000667.2:g.132313652T=	GRCh38
NC_000005.9:g.131649345T= , CM000667.1:g.131649345T=	GRCh37
NC_000005.8:g.131677244T=	NCBI36
NG_012129.1:g.24201T=
NG_012129.2:g.24201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.536T= (SLC22A4) MANE Select	ENSP00000200652.3:p.Val179=
ENST00000200652.3:c.536T= (SLC22A4)	ENSP00000200652.3:p.Val179=
ENST00000491257.1:n.340T= (SLC22A4)
NM_003059.2:c.536T= (SLC22A4)	NP_003050.2:p.Val179=
NR_110997.1:n.825-1399A= (MIR3936HG)
XM_006714675.2:c.8T= (SLC22A4)	XP_006714738.1:p.Val3=
XM_011543589.1:c.432T= (SLC22A4)	XP_011541891.1:p.Cys144=
XM_006714675.4:c.8T= (SLC22A4)	XP_006714738.1:p.Val3=
XM_011543589.2:c.432T= (SLC22A4)	XP_011541891.1:p.Cys144=
XM_017009776.1:c.8T= (SLC22A4)	XP_016865265.1:p.Val3=
NM_003059.3:c.536T= (SLC22A4) MANE Select	NP_003050.2:p.Val179=