Canonical Allele Identifier: CA2347284260

Gene: SLC23A2

Linked Data

• dbSNP Id: rs1012269243

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4976984_4976985dup , CM000682.2:g.4976984_4976985dup	GRCh38
NC_000020.10:g.4957630_4957631dup , CM000682.1:g.4957630_4957631dup	GRCh37
NC_000020.9:g.4905630_4905631dup	NCBI36
NG_029959.1:g.29523_29524dup
NG_029959.2:g.38317_38318dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.-281-6058_-281-6057dup MANE Select	ENSP00000344322.1:n.-281-6058_-281-6057dup
ENST00000338244.5:c.-281-6058_-281-6057dup	ENSP00000344322.1:n.-281-6058_-281-6057dup
ENST00000379333.5:c.-281-6058_-281-6057dup	ENSP00000368637.1:n.-281-6058_-281-6057dup
ENST00000468355.5:n.90-6062_90-6061dup
NM_005116.5:c.-281-6058_-281-6057dup	NP_005107.4:n.-281-6058_-281-6057dup
NM_203327.1:c.-281-6058_-281-6057dup	NP_976072.1:n.-281-6058_-281-6057dup
XM_011529414.1:c.-277-6062_-277-6061dup	XP_011527716.1:n.-277-6062_-277-6061dup
XM_011529417.1:c.-155+24429_-155+24430dup	XP_011527719.1:n.-155+24429_-155+24430dup
NM_005116.6:c.-281-6058_-281-6057dup MANE Select	NP_005107.4:n.-281-6058_-281-6057dup
NM_203327.2:c.-281-6058_-281-6057dup	NP_976072.1:n.-281-6058_-281-6057dup