Canonical Allele Identifier: CA718049802

Gene: LITAF

Linked Data

• dbSNP Id: rs1291912036
• MyVariant Identifiers: chr16:g.11691788G>T (hg19) ; chr16:g.11597932G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11597932G>T , CM000678.2:g.11597932G>T	GRCh38
NC_000016.9:g.11691788G>T , CM000678.1:g.11691788G>T	GRCh37
NC_000016.8:g.11599289G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000571627.5:c.-6+456C>A	ENSP00000460743.1:n.-6+456C>A
ENST00000574848.5:c.85+35601C>A	ENSP00000459898.1:n.85+35601C>A
ENST00000576036.5:c.-6+31191C>A	ENSP00000461667.1:n.-6+31191C>A
ENST00000576334.1:c.85+35601C>A	ENSP00000458538.1:n.85+35601C>A
XM_011522754.1:c.85+35601C>A	XP_011521056.1:n.85+35601C>A
XM_011522754.3:c.85+35601C>A	XP_011521056.1:n.85+35601C>A
XM_017023896.1:c.-6+31191C>A	XP_016879385.1:n.-6+31191C>A