Canonical Allele Identifier: CA2245601035
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996659_6996661delinsTCC , CM000679.2:g.6996659_6996661delinsTCC GRCh38
NC_000017.10:g.6899978_6899980delinsTCC , CM000679.1:g.6899978_6899980delinsTCC GRCh37
NC_000017.9:g.6840702_6840704delinsTCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-167_136-165delinsTCC (ALOX12) MANE Select ENSP00000251535.6:n.136-167_136-165delins...
ENST00000251535.10:c.136-167_136-165delinsTCC (ALOX12) ENSP00000251535.6:n.136-167_136-165delins...
NM_000697.2:c.136-167_136-165delinsTCC (ALOX12) NP_000688.2:n.136-167_136-165delinsTCC
NR_040089.1:n.234-11121_234-11119delinsGGA (ALOX12-AS1)
XM_011523780.1:c.493-167_493-165delinsTCC (ALOX12) XP_011522082.1:n.493-167_493-165delinsTCC...
XM_011523780.2:c.493-167_493-165delinsTCC (ALOX12) XP_011522082.1:n.493-167_493-165delinsTCC...
NM_000697.3:c.136-167_136-165delinsTCC (ALOX12) MANE Select NP_000688.2:n.136-167_136-165delinsTCC