Canonical Allele Identifier: CA2808396176

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075792_8075793insAACACACCCAACACA , CM000679.2:g.8075792_8075793insAACACACCCAACACA	GRCh38
NC_000017.10:g.7979110_7979111insAACACACCCAACACA , CM000679.1:g.7979110_7979111insAACACACCCAACACA	GRCh37
NC_000017.9:g.7919835_7919836insAACACACCCAACACA	NCBI36
NG_007099.1:g.16913_16914insTGTTGGGTGTGTTTG
NG_007099.2:g.16926_16927insTGTTGGGTGTGTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1533-75_1533-74insTGTTGGGTGTGTTTG MANE Select	ENSP00000497784.1:n.1533-75_1533-74insTGTTGGGTGTGTTTG
ENST00000649809.1:c.597-75_597-74insTGTTGGGTGTGTTTG	ENSP00000496845.1:n.597-75_597-74insTGTTGGGTGTGTTTG
ENST00000319144.4:c.1533-75_1533-74insTGTTGGGTGTGTTTG	ENSP00000315167.4:n.1533-75_1533-74insTGTTGGGTGTGTTTG
ENST00000577351.5:n.479+384_479+385insTGTTGGGTGTGTTTG
NM_001139.2:c.1533-75_1533-74insTGTTGGGTGTGTTTG	NP_001130.1:n.1533-75_1533-74insTGTTGGGTGTGTTTG
NM_001139.3:c.1533-75_1533-74insTGTTGGGTGTGTTTG MANE Select	NP_001130.1:n.1533-75_1533-74insTGTTGGGTGTGTTTG