Canonical Allele Identifier: CA1583122967

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132335767G= , CM000667.2:g.132335767G=	GRCh38
NC_000005.9:g.131671460G= , CM000667.1:g.131671460G=	GRCh37
NC_000005.8:g.131699359G=	NCBI36
NG_012129.1:g.46316G=
NG_012129.2:g.46316G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003059.3:c.1262-51G= (SLC22A4) MANE Select	NP_003050.2:n.1262-51G=
ENST00000200652.4:c.1262-51G= (SLC22A4) MANE Select	ENSP00000200652.3:n.1262-51G=
NM_003059.2:c.1262-51G= (SLC22A4)	NP_003050.2:n.1262-51G=
NR_110997.1:n.561-841C= (MIR3936HG)
ENST00000200652.3:c.1262-51G= (SLC22A4)	ENSP00000200652.3:n.1262-51G=
XM_006714675.2:c.734-51G= (SLC22A4)	XP_006714738.1:n.734-51G=
XM_006714675.4:c.734-51G= (SLC22A4)	XP_006714738.1:n.734-51G=
XM_011543589.1:c.986-51G= (SLC22A4)	XP_011541891.1:n.986-51G=
XM_011543589.2:c.986-51G= (SLC22A4)	XP_011541891.1:n.986-51G=
XM_017009776.1:c.734-51G= (SLC22A4)	XP_016865265.1:n.734-51G=