Canonical Allele Identifier: CA2805875721

Gene: LITAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11586049C>A , CM000678.2:g.11586049C>A	GRCh38
NC_000016.9:g.11679905C>A , CM000678.1:g.11679905C>A	GRCh37
NC_000016.8:g.11587406C>A	NCBI36
NG_009008.1:g.5902G>T , LRG_253:g.5902G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001136472.2:c.-6+837G>T MANE Select	NP_001129944.1:n.-6+837G>T
ENST00000622633.5:c.-6+837G>T MANE Select	ENSP00000483114.1:n.-6+837G>T
NM_001136472.1:c.-6+837G>T	NP_001129944.1:n.-6+837G>T
NM_001136473.1:c.-6+837G>T , LRG_253t1:c.-6+837G>T	NP_001129945.1:n.-6+837G>T
NM_004862.3:c.-6+97G>T	NP_004853.2:n.-6+97G>T
NM_004862.4:c.-6+97G>T	NP_004853.2:n.-6+97G>T
NR_024320.1:n.129+1289G>T
NR_024320.2:n.129+1289G>T
ENST00000339430.9:c.-6+97G>T	ENSP00000340118.5:n.-6+97G>T
ENST00000413364.6:c.-6+837G>T	ENSP00000397958.2:n.-6+837G>T
ENST00000570798.5:c.-149+837G>T	ENSP00000458871.1:n.-149+837G>T
ENST00000570904.5:c.-6+1102G>T	ENSP00000459138.1:n.-6+1102G>T
ENST00000571277.1:c.-435+837G>T	ENSP00000459026.1:n.-435+837G>T
ENST00000571459.5:c.-6+837G>T	ENSP00000459603.1:n.-6+837G>T
ENST00000571627.5:c.-6+12339G>T	ENSP00000460743.1:n.-6+12339G>T
ENST00000571688.5:c.-6+1289G>T	ENSP00000459533.1:n.-6+1289G>T
ENST00000571976.1:c.-6+837G>T	ENSP00000460133.1:n.-6+837G>T
ENST00000572255.5:c.-241+837G>T	ENSP00000458836.1:n.-241+837G>T
ENST00000573332.5:c.-6+837G>T	ENSP00000460873.1:n.-6+837G>T
ENST00000574701.5:c.-6+1102G>T	ENSP00000458981.1:n.-6+1102G>T
ENST00000574703.5:c.-6+837G>T	ENSP00000459913.1:n.-6+837G>T
ENST00000574763.5:c.-187+837G>T	ENSP00000461813.1:n.-187+837G>T
ENST00000574848.5:c.86-29314G>T	ENSP00000459898.1:n.86-29314G>T
ENST00000576036.5:c.-5-29314G>T	ENSP00000461667.1:n.-5-29314G>T
ENST00000576334.1:c.86-29314G>T	ENSP00000458538.1:n.86-29314G>T
ENST00000620789.4:c.-6+97G>T	ENSP00000481589.1:n.-6+97G>T
ENST00000622633.4:c.-6+837G>T	ENSP00000483114.1:n.-6+837G>T
XM_006720982.2:c.-6+1102G>T	XP_006721045.1:n.-6+1102G>T
XM_006720982.3:c.-6+1102G>T	XP_006721045.1:n.-6+1102G>T
XM_011522754.1:c.86-29314G>T	XP_011521056.1:n.86-29314G>T
XM_011522754.3:c.86-29314G>T	XP_011521056.1:n.86-29314G>T
XM_017023896.1:c.-5-29314G>T	XP_016879385.1:n.-5-29314G>T