Canonical Allele Identifier: CA1583118062

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313338T= , CM000667.2:g.132313338T=	GRCh38
NC_000005.9:g.131649031T= , CM000667.1:g.131649031T=	GRCh37
NC_000005.8:g.131676930T=	NCBI36
NG_012129.1:g.23887T=
NG_012129.2:g.23887T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-276T= (SLC22A4) MANE Select	ENSP00000200652.3:n.498-276T=
ENST00000200652.3:c.498-276T= (SLC22A4)	ENSP00000200652.3:n.498-276T=
ENST00000491257.1:n.302-276T= (SLC22A4)
NM_003059.2:c.498-276T= (SLC22A4)	NP_003050.2:n.498-276T=
NR_110997.1:n.825-1085A= (MIR3936HG)
XM_006714675.2:c.-31-276T= (SLC22A4)	XP_006714738.1:n.-31-276T=
XM_011543589.1:c.394-276T= (SLC22A4)	XP_011541891.1:n.394-276T=
XM_006714675.4:c.-31-276T= (SLC22A4)	XP_006714738.1:n.-31-276T=
XM_011543589.2:c.394-276T= (SLC22A4)	XP_011541891.1:n.394-276T=
XM_017009776.1:c.-31-276T= (SLC22A4)	XP_016865265.1:n.-31-276T=
NM_003059.3:c.498-276T= (SLC22A4) MANE Select	NP_003050.2:n.498-276T=