Canonical Allele Identifier: CA1583118356

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313651G= , CM000667.2:g.132313651G=	GRCh38
NC_000005.9:g.131649344G= , CM000667.1:g.131649344G=	GRCh37
NC_000005.8:g.131677243G=	NCBI36
NG_012129.1:g.24200G=
NG_012129.2:g.24200G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.535G= (SLC22A4) MANE Select	ENSP00000200652.3:p.Val179=
ENST00000200652.3:c.535G= (SLC22A4)	ENSP00000200652.3:p.Val179=
ENST00000491257.1:n.339G= (SLC22A4)
NM_003059.2:c.535G= (SLC22A4)	NP_003050.2:p.Val179=
NR_110997.1:n.825-1398C= (MIR3936HG)
XM_006714675.2:c.7G= (SLC22A4)	XP_006714738.1:p.Val3=
XM_011543589.1:c.431G= (SLC22A4)	XP_011541891.1:p.Cys144=
XM_006714675.4:c.7G= (SLC22A4)	XP_006714738.1:p.Val3=
XM_011543589.2:c.431G= (SLC22A4)	XP_011541891.1:p.Cys144=
XM_017009776.1:c.7G= (SLC22A4)	XP_016865265.1:p.Val3=
NM_003059.3:c.535G= (SLC22A4) MANE Select	NP_003050.2:p.Val179=