Canonical Allele Identifier: CA13693844

Gene: LTA4H

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.96009832T>C , CM000674.2:g.96009832T>C	GRCh38
NC_000012.11:g.96403610T>C , CM000674.1:g.96403610T>C	GRCh37
NC_000012.10:g.94927741T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228740.7:c.1380-684A>G MANE Select	ENSP00000228740.2:n.1380-684A>G
ENST00000228740.6:c.1380-684A>G	ENSP00000228740.2:n.1380-684A>G
ENST00000413268.6:c.1308-684A>G	ENSP00000395051.2:n.1308-684A>G
ENST00000537111.6:n.1265+162A>G
ENST00000547393.5:n.66-684A>G
ENST00000548375.5:n.489-684A>G
ENST00000548852.5:c.*920-684A>G	ENSP00000449340.1:n.*920-684A>G
ENST00000552789.5:c.1308-684A>G	ENSP00000449958.1:n.1308-684A>G
ENST00000553041.5:n.4813A>G
NM_000895.2:c.1380-684A>G	NP_000886.1:n.1380-684A>G
NM_001256643.1:c.1308-684A>G	NP_001243572.1:n.1308-684A>G
NM_001256644.1:c.1308-684A>G	NP_001243573.1:n.1308-684A>G
NR_132659.1:n.1461-684A>G
XM_005268871.1:c.1380-684A>G	XP_005268928.1:n.1380-684A>G
XM_011538348.1:c.1380-684A>G	XP_011536650.1:n.1380-684A>G
XM_011538349.1:c.*1970A>G	XP_011536651.1:n.*1970A>G
XR_945235.1:n.815-129T>C
XR_945236.1:n.777-129T>C
XR_945237.1:n.453-129T>C
XM_005268871.2:c.1380-684A>G	XP_005268928.1:n.1380-684A>G
XR_001748703.2:n.1481-684A>G
XR_001749274.2:n.1962-129T>C
XR_001749275.2:n.410-129T>C
XR_002957326.1:n.1481-684A>G
XR_002957423.1:n.87-129T>C
XR_002957424.1:n.240-129T>C
XR_945236.3:n.831-129T>C
XR_945237.3:n.507-129T>C
NM_000895.3:c.1380-684A>G MANE Select	NP_000886.1:n.1380-684A>G
NR_132659.2:n.1387-684A>G