Canonical Allele Identifier: CA2245601067
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996692_6996693delinsCG , CM000679.2:g.6996692_6996693delinsCG GRCh38
NC_000017.10:g.6900011_6900012delinsCG , CM000679.1:g.6900011_6900012delinsCG GRCh37
NC_000017.9:g.6840735_6840736delinsCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-134_136-133delinsCG (ALOX12) MANE Select ENSP00000251535.6:n.136-134_136-133delinsCG
ENST00000251535.10:c.136-134_136-133delinsCG (ALOX12) ENSP00000251535.6:n.136-134_136-133delinsCG
NM_000697.2:c.136-134_136-133delinsCG (ALOX12) NP_000688.2:n.136-134_136-133delinsCG
NR_040089.1:n.234-11153_234-11152delinsCG (ALOX12-AS1)
XM_011523780.1:c.493-134_493-133delinsCG (ALOX12) XP_011522082.1:n.493-134_493-133delinsCG
XM_011523780.2:c.493-134_493-133delinsCG (ALOX12) XP_011522082.1:n.493-134_493-133delinsCG
NM_000697.3:c.136-134_136-133delinsCG (ALOX12) MANE Select NP_000688.2:n.136-134_136-133delinsCG