Canonical Allele Identifier: CA497599068

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-6996957-C-T
• COSMIC: COSM5004593
• MyVariant Identifiers: chr17:g.6900276C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996957C>T , CM000679.2:g.6996957C>T	GRCh38
NC_000017.10:g.6900276C>T , CM000679.1:g.6900276C>T	GRCh37
NC_000017.9:g.6841000C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.267C>T (ALOX12) MANE Select	ENSP00000251535.6:p.Cys89=
ENST00000251535.10:c.267C>T (ALOX12)	ENSP00000251535.6:p.Cys89=
NM_000697.2:c.267C>T (ALOX12)	NP_000688.2:p.Cys89=
NR_040089.1:n.234-11417G>A (ALOX12-AS1)
XM_011523780.1:c.624C>T (ALOX12)	XP_011522082.1:p.Cys208=
XM_011523780.2:c.624C>T (ALOX12)	XP_011522082.1:p.Cys208=
NM_000697.3:c.267C>T (ALOX12) MANE Select	NP_000688.2:p.Cys89=