Canonical Allele Identifier: CA2347284258

Gene: SLC23A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4976975_4976976delinsCA , CM000682.2:g.4976975_4976976delinsCA	GRCh38
NC_000020.10:g.4957621_4957622delinsCA , CM000682.1:g.4957621_4957622delinsCA	GRCh37
NC_000020.9:g.4905621_4905622delinsCA	NCBI36
NG_029959.1:g.29524_29525delinsTG
NG_029959.2:g.38318_38319delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.-281-6057_-281-6056delinsTG MANE Select	ENSP00000344322.1:n.-281-6057_-281-6056delinsTG
ENST00000338244.5:c.-281-6057_-281-6056delinsTG	ENSP00000344322.1:n.-281-6057_-281-6056delinsTG
ENST00000379333.5:c.-281-6057_-281-6056delinsTG	ENSP00000368637.1:n.-281-6057_-281-6056delinsTG
ENST00000468355.5:n.90-6061_90-6060delinsTG
NM_005116.5:c.-281-6057_-281-6056delinsTG	NP_005107.4:n.-281-6057_-281-6056delinsTG
NM_203327.1:c.-281-6057_-281-6056delinsTG	NP_976072.1:n.-281-6057_-281-6056delinsTG
XM_011529414.1:c.-277-6061_-277-6060delinsTG	XP_011527716.1:n.-277-6061_-277-6060delinsTG
XM_011529417.1:c.-155+24430_-155+24431delinsTG	XP_011527719.1:n.-155+24430_-155+24431delinsTG
NM_005116.6:c.-281-6057_-281-6056delinsTG MANE Select	NP_005107.4:n.-281-6057_-281-6056delinsTG
NM_203327.2:c.-281-6057_-281-6056delinsTG	NP_976072.1:n.-281-6057_-281-6056delinsTG