Canonical Allele Identifier: CA2635747830
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001943_7001944insCAAGATAT , CM000679.2:g.7001943_7001944insCAAGATAT GRCh38
NC_000017.10:g.6905262_6905263insCAAGATAT , CM000679.1:g.6905262_6905263insCAAGATAT GRCh37
NC_000017.9:g.6845986_6845987insCAAGATAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+132_1161+133insCAAGATAT (ALOX12) MANE Select ENSP00000251535.6:n.1161+132_1161+133insCAAGATAT
ENST00000251535.10:c.1161+132_1161+133insCAAGATAT (ALOX12) ENSP00000251535.6:n.1161+132_1161+133insCAAGATAT
NM_000697.2:c.1161+132_1161+133insCAAGATAT (ALOX12) NP_000688.2:n.1161+132_1161+133insCAAGATAT
NR_040089.1:n.233+7853_233+7854insTATCTTGA (ALOX12-AS1)
XM_011523780.1:c.1311+132_1311+133insCAAGATAT (ALOX12) XP_011522082.1:n.1311+132_1311+133insCAAGATAT
XM_011523780.2:c.1311+132_1311+133insCAAGATAT (ALOX12) XP_011522082.1:n.1311+132_1311+133insCAAGATAT
NM_000697.3:c.1161+132_1161+133insCAAGATAT (ALOX12) MANE Select NP_000688.2:n.1161+132_1161+133insCAAGATAT