Canonical Allele Identifier: CA2056504578

Gene: LTA4H

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.96015423A= , CM000674.2:g.96015423A=	GRCh38
NC_000012.11:g.96409201A= , CM000674.1:g.96409201A=	GRCh37
NC_000012.10:g.94933332A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000895.3:c.1059+160T= MANE Select	NP_000886.1:n.1059+160T=
ENST00000228740.7:c.1059+160T= MANE Select	ENSP00000228740.2:n.1059+160T=
NM_000895.2:c.1059+160T=	NP_000886.1:n.1059+160T=
NM_001256643.1:c.987+160T=	NP_001243572.1:n.987+160T=
NM_001256644.1:c.987+160T=	NP_001243573.1:n.987+160T=
NR_132659.1:n.1140+160T=
NR_132659.2:n.1066+160T=
ENST00000228740.6:c.1059+160T=	ENSP00000228740.2:n.1059+160T=
ENST00000413268.6:c.987+160T=	ENSP00000395051.2:n.987+160T=
ENST00000548852.5:c.*599+160T=	ENSP00000449340.1:n.*599+160T=
ENST00000552789.5:c.987+160T=	ENSP00000449958.1:n.987+160T=
ENST00000553041.5:n.1137+160T=
XM_005268871.1:c.1059+160T=	XP_005268928.1:n.1059+160T=
XM_005268871.2:c.1059+160T=	XP_005268928.1:n.1059+160T=
XM_011538348.1:c.1059+160T=	XP_011536650.1:n.1059+160T=
XM_011538349.1:c.1059+160T=	XP_011536651.1:n.1059+160T=
XM_011538349.3:c.1059+160T=	XP_011536651.1:n.1059+160T=
XR_001748703.2:n.1160+160T=
XR_002957326.1:n.1160+160T=