Canonical Allele Identifier: CA2207719509

Gene: LITAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11597831G= , CM000678.2:g.11597831G=	GRCh38
NC_000016.9:g.11691687G= , CM000678.1:g.11691687G=	GRCh37
NC_000016.8:g.11599188G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000571627.5:c.-6+557C=	ENSP00000460743.1:n.-6+557C=
ENST00000574848.5:c.85+35702C=	ENSP00000459898.1:n.85+35702C=
ENST00000576036.5:c.-6+31292C=	ENSP00000461667.1:n.-6+31292C=
ENST00000576334.1:c.85+35702C=	ENSP00000458538.1:n.85+35702C=
XM_011522754.1:c.85+35702C=	XP_011521056.1:n.85+35702C=
XM_011522754.3:c.85+35702C=	XP_011521056.1:n.85+35702C=
XM_017023896.1:c.-6+31292C=	XP_016879385.1:n.-6+31292C=