Canonical Allele Identifier: CA2056511106
Gene: LTA4H HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.96036605_96036606delinsAG , CM000674.2:g.96036605_96036606delinsAG GRCh38
NC_000012.11:g.96430383_96430384delinsAG , CM000674.1:g.96430383_96430384delinsAG GRCh37
NC_000012.10:g.94954514_94954515delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000413268.6:c.87+6683_87+6684delinsCT ENSP00000395051.2:n.87+6683_87+6684delins...
ENST00000552789.5:c.87+6683_87+6684delinsCT ENSP00000449958.1:n.87+6683_87+6684delins...
NM_001256643.1:c.87+6683_87+6684delinsCT NP_001243572.1:n.87+6683_87+6684delinsCT
NM_001256644.1:c.87+6683_87+6684delinsCT NP_001243573.1:n.87+6683_87+6684delinsCT