Canonical Allele Identifier: CA1583125036

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340640T= , CM000667.2:g.132340640T=	GRCh38
NC_000005.9:g.131676333T= , CM000667.1:g.131676333T=	GRCh37
NC_000005.8:g.131704232T=	NCBI36
NG_012129.1:g.51189T=
NG_012129.2:g.51189T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1520T= (SLC22A4) MANE Select	ENSP00000200652.3:p.Phe507=
ENST00000200652.3:c.1520T= (SLC22A4)	ENSP00000200652.3:p.Phe507=
NM_003059.2:c.1520T= (SLC22A4)	NP_003050.2:p.Phe507=
NR_110997.1:n.561-5714A= (MIR3936HG)
XM_006714675.2:c.992T= (SLC22A4)	XP_006714738.1:p.Phe331=
XM_011543589.1:c.1244T= (SLC22A4)	XP_011541891.1:p.Phe415=
XM_006714675.4:c.992T= (SLC22A4)	XP_006714738.1:p.Phe331=
XM_011543589.2:c.1244T= (SLC22A4)	XP_011541891.1:p.Phe415=
XM_017009776.1:c.992T= (SLC22A4)	XP_016865265.1:p.Phe331=
NM_003059.3:c.1520T= (SLC22A4) MANE Select	NP_003050.2:p.Phe507=