Canonical Allele Identifier: CA2815122206

Gene: SLC23A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4910984dup , CM000682.2:g.4910984dup	GRCh38
NC_000020.10:g.4891630dup , CM000682.1:g.4891630dup	GRCh37
NC_000020.9:g.4839630dup	NCBI36
NG_029959.1:g.95519dup
NG_029959.2:g.104313dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.207+1899dup MANE Select	ENSP00000344322.1:n.207+1899dup
ENST00000338244.5:c.207+1899dup	ENSP00000344322.1:n.207+1899dup
ENST00000379333.5:c.207+1899dup	ENSP00000368637.1:n.207+1899dup
ENST00000468355.5:n.573+1899dup
NM_005116.5:c.207+1899dup	NP_005107.4:n.207+1899dup
NM_203327.1:c.207+1899dup	NP_976072.1:n.207+1899dup
XM_011529414.1:c.207+1899dup	XP_011527716.1:n.207+1899dup
XM_011529415.1:c.207+1899dup	XP_011527717.1:n.207+1899dup
XM_011529416.1:c.207+1899dup	XP_011527718.1:n.207+1899dup
XM_011529417.1:c.207+1899dup	XP_011527719.1:n.207+1899dup
NM_005116.6:c.207+1899dup MANE Select	NP_005107.4:n.207+1899dup
NM_203327.2:c.207+1899dup	NP_976072.1:n.207+1899dup