Canonical Allele Identifier: CA624676573
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1485624462
gnomAD v2: 17-6905281-TAA-T
gnomAD v3: 17-7001962-TAA-T
gnomAD v4: 17-7001962-TAA-T
MyVariant Identifiers: chr17:g.6905282_6905283del (hg19) chr17:g.7001963_7001964del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001963_7001964del , CM000679.2:g.7001963_7001964del GRCh38
NC_000017.10:g.6905282_6905283del , CM000679.1:g.6905282_6905283del GRCh37
NC_000017.9:g.6846006_6846007del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+152_1161+153del (ALOX12) MANE Select ENSP00000251535.6:n.1161+152_1161+153del
ENST00000251535.10:c.1161+152_1161+153del (ALOX12) ENSP00000251535.6:n.1161+152_1161+153del
NM_000697.2:c.1161+152_1161+153del (ALOX12) NP_000688.2:n.1161+152_1161+153del
NR_040089.1:n.233+7832_233+7833del (ALOX12-AS1)
XM_011523780.1:c.1311+152_1311+153del (ALOX12) XP_011522082.1:n.1311+152_1311+153del
XM_011523780.2:c.1311+152_1311+153del (ALOX12) XP_011522082.1:n.1311+152_1311+153del
NM_000697.3:c.1161+152_1161+153del (ALOX12) MANE Select NP_000688.2:n.1161+152_1161+153del
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