Canonical Allele Identifier: CA1583107912

Gene: SLC22A4

Linked Data

• dbSNP Id: rs1480176254

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132297666T>G , CM000667.2:g.132297666T>G	GRCh38
NC_000005.9:g.131633359T>G , CM000667.1:g.131633359T>G	GRCh37
NC_000005.8:g.131661258T>G	NCBI36
NG_012129.1:g.8215T>G
NG_012129.2:g.8215T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.393+2657T>G MANE Select	ENSP00000200652.3:n.393+2657T>G
ENST00000200652.3:c.393+2657T>G	ENSP00000200652.3:n.393+2657T>G
ENST00000491257.1:n.197+2045T>G
NM_003059.2:c.393+2657T>G	NP_003050.2:n.393+2657T>G
XM_006714675.2:c.-32+2657T>G	XP_006714738.1:n.-32+2657T>G
XM_011543589.1:c.393+2657T>G	XP_011541891.1:n.393+2657T>G
XR_948289.1:n.1238+2045T>G
XM_006714675.4:c.-32+2657T>G	XP_006714738.1:n.-32+2657T>G
XM_011543589.2:c.393+2657T>G	XP_011541891.1:n.393+2657T>G
XM_017009776.1:c.-136+2045T>G	XP_016865265.1:n.-136+2045T>G
NM_003059.3:c.393+2657T>G MANE Select	NP_003050.2:n.393+2657T>G