Canonical Allele Identifier: CA804002478

Gene: SLC22A4 MIR3936HG

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132324738A>G , CM000667.2:g.132324738A>G	GRCh38
NC_000005.9:g.131660431A>G , CM000667.1:g.131660431A>G	GRCh37
NC_000005.8:g.131688330A>G	NCBI36
NG_012129.1:g.35287A>G
NG_012129.2:g.35287A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.824+2383A>G (SLC22A4) MANE Select	ENSP00000200652.3:n.824+2383A>G
ENST00000200652.3:c.824+2383A>G (SLC22A4)	ENSP00000200652.3:n.824+2383A>G
ENST00000425923.1:n.354+96A>G (SLC22A4)
NM_003059.2:c.824+2383A>G (SLC22A4)	NP_003050.2:n.824+2383A>G
NR_110997.1:n.824+7451T>C (MIR3936HG)
XM_006714675.2:c.296+2383A>G (SLC22A4)	XP_006714738.1:n.296+2383A>G
XM_011543589.1:c.549-2539A>G (SLC22A4)	XP_011541891.1:n.549-2539A>G
XM_006714675.4:c.296+2383A>G (SLC22A4)	XP_006714738.1:n.296+2383A>G
XM_011543589.2:c.549-2539A>G (SLC22A4)	XP_011541891.1:n.549-2539A>G
XM_017009776.1:c.296+2383A>G (SLC22A4)	XP_016865265.1:n.296+2383A>G
NM_003059.3:c.824+2383A>G (SLC22A4) MANE Select	NP_003050.2:n.824+2383A>G