Canonical Allele Identifier: CA2505923382

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997099_6997100insAAAGGGGG , CM000679.2:g.6997099_6997100insAAAGGGGG	GRCh38
NC_000017.10:g.6900418_6900419insAAAGGGGG , CM000679.1:g.6900418_6900419insAAAGGGGG	GRCh37
NC_000017.9:g.6841142_6841143insAAAGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.337+72_337+73insAAAGGGGG (ALOX12) MANE Select	ENSP00000251535.6:n.337+72_337+73insAAAGGGGG
ENST00000251535.10:c.337+72_337+73insAAAGGGGG (ALOX12)	ENSP00000251535.6:n.337+72_337+73insAAAGGGGG
ENST00000480801.1:c.46+72_46+73insAAAGGGGG (ALOX12)	ENSP00000467033.1:n.46+72_46+73insAAAGGGGG
NM_000697.2:c.337+72_337+73insAAAGGGGG (ALOX12)	NP_000688.2:n.337+72_337+73insAAAGGGGG
NR_040089.1:n.234-11560_234-11559insCCCCCTTT (ALOX12-AS1)
XM_011523780.1:c.694+72_694+73insAAAGGGGG (ALOX12)	XP_011522082.1:n.694+72_694+73insAAAGGGGG
XM_011523780.2:c.694+72_694+73insAAAGGGGG (ALOX12)	XP_011522082.1:n.694+72_694+73insAAAGGGGG
NM_000697.3:c.337+72_337+73insAAAGGGGG (ALOX12) MANE Select	NP_000688.2:n.337+72_337+73insAAAGGGGG