Canonical Allele Identifier: CA1583117644

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132327369T= , CM000667.2:g.132327369T=	GRCh38
NC_000005.9:g.131663062T= , CM000667.1:g.131663062T=	GRCh37
NC_000005.8:g.131690961T=	NCBI36
NG_012129.1:g.37918T=
NG_012129.2:g.37918T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003059.3:c.917T= (SLC22A4) MANE Select	NP_003050.2:p.Ile306=
ENST00000200652.4:c.917T= (SLC22A4) MANE Select	ENSP00000200652.3:p.Ile306=
NM_003059.2:c.917T= (SLC22A4)	NP_003050.2:p.Ile306=
NR_110997.1:n.824+4820A= (MIR3936HG)
ENST00000200652.3:c.917T= (SLC22A4)	ENSP00000200652.3:p.Ile306=
ENST00000425923.1:n.447T= (SLC22A4)
XM_006714675.2:c.389T= (SLC22A4)	XP_006714738.1:p.Ile130=
XM_006714675.4:c.389T= (SLC22A4)	XP_006714738.1:p.Ile130=
XM_011543589.1:c.641T= (SLC22A4)	XP_011541891.1:p.Ile214=
XM_011543589.2:c.641T= (SLC22A4)	XP_011541891.1:p.Ile214=
XM_017009776.1:c.389T= (SLC22A4)	XP_016865265.1:p.Ile130=