Canonical Allele Identifier: CA1014983816

Gene: SLC23A2

Linked Data

• gnomAD v3: 20-4976965-AGCTCCATCTC-A
• gnomAD v4: 20-4976965-AGCTCCATCTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4976966_4976975del , CM000682.2:g.4976966_4976975del	GRCh38
NC_000020.10:g.4957612_4957621del , CM000682.1:g.4957612_4957621del	GRCh37
NC_000020.9:g.4905612_4905621del	NCBI36
NG_029959.1:g.29525_29534del
NG_029959.2:g.38319_38328del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.-281-6056_-281-6047del MANE Select	ENSP00000344322.1:n.-281-6056_-281-6047del
ENST00000338244.5:c.-281-6056_-281-6047del	ENSP00000344322.1:n.-281-6056_-281-6047del
ENST00000379333.5:c.-281-6056_-281-6047del	ENSP00000368637.1:n.-281-6056_-281-6047del
ENST00000468355.5:n.90-6060_90-6051del
NM_005116.5:c.-281-6056_-281-6047del	NP_005107.4:n.-281-6056_-281-6047del
NM_203327.1:c.-281-6056_-281-6047del	NP_976072.1:n.-281-6056_-281-6047del
XM_011529414.1:c.-277-6060_-277-6051del	XP_011527716.1:n.-277-6060_-277-6051del
XM_011529417.1:c.-155+24431_-155+24440del	XP_011527719.1:n.-155+24431_-155+24440del
NM_005116.6:c.-281-6056_-281-6047del MANE Select	NP_005107.4:n.-281-6056_-281-6047del
NM_203327.2:c.-281-6056_-281-6047del	NP_976072.1:n.-281-6056_-281-6047del