Canonical Allele Identifier: CA2635747833
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001948del , CM000679.2:g.7001948del GRCh38
NC_000017.10:g.6905267del , CM000679.1:g.6905267del GRCh37
NC_000017.9:g.6845991del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+137del (ALOX12) MANE Select ENSP00000251535.6:n.1161+137del
ENST00000251535.10:c.1161+137del (ALOX12) ENSP00000251535.6:n.1161+137del
NM_000697.2:c.1161+137del (ALOX12) NP_000688.2:n.1161+137del
NR_040089.1:n.233+7848del (ALOX12-AS1)
XM_011523780.1:c.1311+137del (ALOX12) XP_011522082.1:n.1311+137del
XM_011523780.2:c.1311+137del (ALOX12) XP_011522082.1:n.1311+137del
NM_000697.3:c.1161+137del (ALOX12) MANE Select NP_000688.2:n.1161+137del