Canonical Allele Identifier: CA2580575674
Gene: LITAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11597897T>A , CM000678.2:g.11597897T>A GRCh38
NC_000016.9:g.11691753T>A , CM000678.1:g.11691753T>A GRCh37
NC_000016.8:g.11599254T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000571627.5:c.-6+491A>T ENSP00000460743.1:n.-6+491A>T
ENST00000574848.5:c.85+35636A>T ENSP00000459898.1:n.85+35636A>T
ENST00000576036.5:c.-6+31226A>T ENSP00000461667.1:n.-6+31226A>T
ENST00000576334.1:c.85+35636A>T ENSP00000458538.1:n.85+35636A>T
XM_011522754.1:c.85+35636A>T XP_011521056.1:n.85+35636A>T
XM_011522754.3:c.85+35636A>T XP_011521056.1:n.85+35636A>T
XM_017023896.1:c.-6+31226A>T XP_016879385.1:n.-6+31226A>T