Canonical Allele Identifier: CA1583107920

Gene: SLC22A4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132297674_132297678delinsGAAAA , CM000667.2:g.132297674_132297678delinsGAAAA	GRCh38
NC_000005.9:g.131633367_131633371delinsGAAAA , CM000667.1:g.131633367_131633371delinsGAAAA	GRCh37
NC_000005.8:g.131661266_131661270delinsGAAAA	NCBI36
NG_012129.1:g.8223_8227delinsGAAAA
NG_012129.2:g.8223_8227delinsGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.393+2665_393+2669delinsGAAAA MANE Select	ENSP00000200652.3:n.393+2665_393+2669delinsGAAAA
ENST00000200652.3:c.393+2665_393+2669delinsGAAAA	ENSP00000200652.3:n.393+2665_393+2669delinsGAAAA
ENST00000491257.1:n.197+2053_197+2057delinsGAAAA
NM_003059.2:c.393+2665_393+2669delinsGAAAA	NP_003050.2:n.393+2665_393+2669delinsGAAAA
XM_006714675.2:c.-32+2665_-32+2669delinsGAAAA	XP_006714738.1:n.-32+2665_-32+2669delinsGAAAA
XM_011543589.1:c.393+2665_393+2669delinsGAAAA	XP_011541891.1:n.393+2665_393+2669delinsGAAAA
XR_948289.1:n.1238+2053_1238+2057delinsGAAAA
XM_006714675.4:c.-32+2665_-32+2669delinsGAAAA	XP_006714738.1:n.-32+2665_-32+2669delinsGAAAA
XM_011543589.2:c.393+2665_393+2669delinsGAAAA	XP_011541891.1:n.393+2665_393+2669delinsGAAAA
XM_017009776.1:c.-136+2053_-136+2057delinsGAAAA	XP_016865265.1:n.-136+2053_-136+2057delinsGAAAA
NM_003059.3:c.393+2665_393+2669delinsGAAAA MANE Select	NP_003050.2:n.393+2665_393+2669delinsGAAAA