Canonical Allele Identifier: CA2245576082
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001604_7001618delinsTCAGCCTCCCAACCC , CM000679.2:g.7001604_7001618delinsTCAGCCTCCCAACCC GRCh38
NC_000017.10:g.6904923_6904937delinsTCAGCCTCCCAACCC , CM000679.1:g.6904923_6904937delinsTCAGCCTCCCAACCC GRCh37
NC_000017.9:g.6845647_6845661delinsTCAGCCTCCCAACCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.954_968delinsTCAGCCTCCCAACCC (ALOX12) MANE Select ENSP00000251535.6:p.Ile318=
ENST00000251535.10:c.954_968delinsTCAGCCTCCCAACCC (ALOX12) ENSP00000251535.6:p.Ile318=
NM_000697.2:c.954_968delinsTCAGCCTCCCAACCC (ALOX12) NP_000688.2:p.Ile318=
NR_040089.1:n.233+8178_233+8192delinsGGGTTGGGAGGCTGA (ALOX12-AS1)
XM_011523780.1:c.1104_1118delinsTCAGCCTCCCAACCC (ALOX12) XP_011522082.1:p.Ile368=
XM_011523780.2:c.1104_1118delinsTCAGCCTCCCAACCC (ALOX12) XP_011522082.1:p.Ile368=
NM_000697.3:c.954_968delinsTCAGCCTCCCAACCC (ALOX12) MANE Select NP_000688.2:p.Ile318=