Canonical Allele Identifier: CA497599102

Gene: ALOX12 ALOX12-AS1

Linked Data

• MyVariant Identifiers: chr17:g.6900333G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997014G>C , CM000679.2:g.6997014G>C	GRCh38
NC_000017.10:g.6900333G>C , CM000679.1:g.6900333G>C	GRCh37
NC_000017.9:g.6841057G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.324G>C (ALOX12) MANE Select	ENSP00000251535.6:p.Leu108=
ENST00000251535.10:c.324G>C (ALOX12)	ENSP00000251535.6:p.Leu108=
ENST00000480801.1:c.33G>C (ALOX12)	ENSP00000467033.1:p.Leu11=
NM_000697.2:c.324G>C (ALOX12)	NP_000688.2:p.Leu108=
NR_040089.1:n.234-11474C>G (ALOX12-AS1)
XM_011523780.1:c.681G>C (ALOX12)	XP_011522082.1:p.Leu227=
XM_011523780.2:c.681G>C (ALOX12)	XP_011522082.1:p.Leu227=
NM_000697.3:c.324G>C (ALOX12) MANE Select	NP_000688.2:p.Leu108=