Canonical Allele Identifier: CA1583107911

Gene: SLC22A4

Genomic Alleles

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

Transcript Alleles

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