Canonical Allele Identifier: CA2207719507
Gene: LITAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11597826G= , CM000678.2:g.11597826G= GRCh38
NC_000016.9:g.11691682G= , CM000678.1:g.11691682G= GRCh37
NC_000016.8:g.11599183G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000571627.5:c.-6+562C= ENSP00000460743.1:n.-6+562C=
ENST00000574848.5:c.85+35707C= ENSP00000459898.1:n.85+35707C=
ENST00000576036.5:c.-6+31297C= ENSP00000461667.1:n.-6+31297C=
ENST00000576334.1:c.85+35707C= ENSP00000458538.1:n.85+35707C=
XM_011522754.1:c.85+35707C= XP_011521056.1:n.85+35707C=
XM_011522754.3:c.85+35707C= XP_011521056.1:n.85+35707C=
XM_017023896.1:c.-6+31297C= XP_016879385.1:n.-6+31297C=