Canonical Allele Identifier: CA2635962142

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8086279-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086279_8086280insTT , CM000679.2:g.8086279_8086280insTT	GRCh38
NC_000017.10:g.7989597_7989598insTT , CM000679.1:g.7989597_7989598insTT	GRCh37
NC_000017.9:g.7930322_7930323insTT	NCBI36
NG_007099.1:g.6424_6425insAA
NG_007099.2:g.6437_6438insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-60_148-59insAA MANE Select	ENSP00000497784.1:n.148-60_148-59insAA
ENST00000319144.4:c.148-60_148-59insAA	ENSP00000315167.4:n.148-60_148-59insAA
NM_001139.2:c.148-60_148-59insAA	NP_001130.1:n.148-60_148-59insAA
NM_001139.3:c.148-60_148-59insAA MANE Select	NP_001130.1:n.148-60_148-59insAA