Canonical Allele Identifier: CA2635959443

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8076506-T-TGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076506_8076507insGCC , CM000679.2:g.8076506_8076507insGCC	GRCh38
NC_000017.10:g.7979824_7979825insGCC , CM000679.1:g.7979824_7979825insGCC	GRCh37
NC_000017.9:g.7920549_7920550insGCC	NCBI36
NG_007099.1:g.16197_16198insGGC
NG_007099.2:g.16210_16211insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+150_1362+151insGGC MANE Select	ENSP00000497784.1:n.1362+150_1362+151insGGC
ENST00000649809.1:c.426+150_426+151insGGC	ENSP00000496845.1:n.426+150_426+151insGGC
ENST00000319144.4:c.1362+150_1362+151insGGC	ENSP00000315167.4:n.1362+150_1362+151insGGC
ENST00000577351.5:n.309+150_309+151insGGC
ENST00000583276.5:n.746+150_746+151insGGC
ENST00000584116.1:n.618+150_618+151insGGC
NM_001139.2:c.1362+150_1362+151insGGC	NP_001130.1:n.1362+150_1362+151insGGC
NM_001139.3:c.1362+150_1362+151insGGC MANE Select	NP_001130.1:n.1362+150_1362+151insGGC