Canonical Allele Identifier: CA2245576054
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001553_7001556delinsTATA , CM000679.2:g.7001553_7001556delinsTATA GRCh38
NC_000017.10:g.6904872_6904875delinsTATA , CM000679.1:g.6904872_6904875delinsTATA GRCh37
NC_000017.9:g.6845596_6845599delinsTATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.952-49_952-46delinsTATA (ALOX12) MANE Select ENSP00000251535.6:n.952-49_952-46delinsTATA
ENST00000251535.10:c.952-49_952-46delinsTATA (ALOX12) ENSP00000251535.6:n.952-49_952-46delinsTATA
NM_000697.2:c.952-49_952-46delinsTATA (ALOX12) NP_000688.2:n.952-49_952-46delinsTATA
NR_040089.1:n.233+8240_233+8243delinsTATA (ALOX12-AS1)
XM_011523780.1:c.1102-49_1102-46delinsTATA (ALOX12) XP_011522082.1:n.1102-49_1102-46delinsTATA
XM_011523780.2:c.1102-49_1102-46delinsTATA (ALOX12) XP_011522082.1:n.1102-49_1102-46delinsTATA
NM_000697.3:c.952-49_952-46delinsTATA (ALOX12) MANE Select NP_000688.2:n.952-49_952-46delinsTATA