Canonical Allele Identifier: CA2576145323
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001583_7001584del , CM000679.2:g.7001583_7001584del GRCh38
NC_000017.10:g.6904902_6904903del , CM000679.1:g.6904902_6904903del GRCh37
NC_000017.9:g.6845626_6845627del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.952-19_952-18del (ALOX12) MANE Select ENSP00000251535.6:n.952-19_952-18del
ENST00000251535.10:c.952-19_952-18del (ALOX12) ENSP00000251535.6:n.952-19_952-18del
NM_000697.2:c.952-19_952-18del (ALOX12) NP_000688.2:n.952-19_952-18del
NR_040089.1:n.233+8213_233+8214del (ALOX12-AS1)
XM_011523780.1:c.1102-19_1102-18del (ALOX12) XP_011522082.1:n.1102-19_1102-18del
XM_011523780.2:c.1102-19_1102-18del (ALOX12) XP_011522082.1:n.1102-19_1102-18del
NM_000697.3:c.952-19_952-18del (ALOX12) MANE Select NP_000688.2:n.952-19_952-18del