Canonical Allele Identifier: CA1583118456

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313730T= , CM000667.2:g.132313730T=	GRCh38
NC_000005.9:g.131649423T= , CM000667.1:g.131649423T=	GRCh37
NC_000005.8:g.131677322T=	NCBI36
NG_012129.1:g.24279T=
NG_012129.2:g.24279T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.614T= (SLC22A4) MANE Select	ENSP00000200652.3:p.Met205=
ENST00000200652.3:c.614T= (SLC22A4)	ENSP00000200652.3:p.Met205=
ENST00000491257.1:n.418T= (SLC22A4)
NM_003059.2:c.614T= (SLC22A4)	NP_003050.2:p.Met205=
NR_110997.1:n.825-1477A= (MIR3936HG)
XM_006714675.2:c.86T= (SLC22A4)	XP_006714738.1:p.Met29=
XM_011543589.1:c.510T= (SLC22A4)	XP_011541891.1:p.His170=
XM_006714675.4:c.86T= (SLC22A4)	XP_006714738.1:p.Met29=
XM_011543589.2:c.510T= (SLC22A4)	XP_011541891.1:p.His170=
XM_017009776.1:c.86T= (SLC22A4)	XP_016865265.1:p.Met29=
NM_003059.3:c.614T= (SLC22A4) MANE Select	NP_003050.2:p.Met205=