Canonical Allele Identifier: CA2245576148
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001768T= , CM000679.2:g.7001768T= GRCh38
NC_000017.10:g.6905087T= , CM000679.1:g.6905087T= GRCh37
NC_000017.9:g.6845811T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1118T= (ALOX12) MANE Select ENSP00000251535.6:p.Val373=
ENST00000251535.10:c.1118T= (ALOX12) ENSP00000251535.6:p.Val373=
NM_000697.2:c.1118T= (ALOX12) NP_000688.2:p.Val373=
NR_040089.1:n.233+8028A= (ALOX12-AS1)
XM_011523780.1:c.1268T= (ALOX12) XP_011522082.1:p.Val423=
XM_011523780.2:c.1268T= (ALOX12) XP_011522082.1:p.Val423=
NM_000697.3:c.1118T= (ALOX12) MANE Select NP_000688.2:p.Val373=
Search 100 bp 5'
Search 100 bp 3'