Canonical Allele Identifier: CA1583107919

Gene: SLC22A4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132297673_132297674delinsAG , CM000667.2:g.132297673_132297674delinsAG	GRCh38
NC_000005.9:g.131633366_131633367delinsAG , CM000667.1:g.131633366_131633367delinsAG	GRCh37
NC_000005.8:g.131661265_131661266delinsAG	NCBI36
NG_012129.1:g.8222_8223delinsAG
NG_012129.2:g.8222_8223delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.393+2664_393+2665delinsAG MANE Select	ENSP00000200652.3:n.393+2664_393+2665delinsAG
ENST00000200652.3:c.393+2664_393+2665delinsAG	ENSP00000200652.3:n.393+2664_393+2665delinsAG
ENST00000491257.1:n.197+2052_197+2053delinsAG
NM_003059.2:c.393+2664_393+2665delinsAG	NP_003050.2:n.393+2664_393+2665delinsAG
XM_006714675.2:c.-32+2664_-32+2665delinsAG	XP_006714738.1:n.-32+2664_-32+2665delinsAG
XM_011543589.1:c.393+2664_393+2665delinsAG	XP_011541891.1:n.393+2664_393+2665delinsAG
XR_948289.1:n.1238+2052_1238+2053delinsAG
XM_006714675.4:c.-32+2664_-32+2665delinsAG	XP_006714738.1:n.-32+2664_-32+2665delinsAG
XM_011543589.2:c.393+2664_393+2665delinsAG	XP_011541891.1:n.393+2664_393+2665delinsAG
XM_017009776.1:c.-136+2052_-136+2053delinsAG	XP_016865265.1:n.-136+2052_-136+2053delinsAG
NM_003059.3:c.393+2664_393+2665delinsAG MANE Select	NP_003050.2:n.393+2664_393+2665delinsAG