Canonical Allele Identifier: CA621177076

Gene: LITAF

Linked Data

• dbSNP Id: rs1371045707
• gnomAD v2: 16-11647567-AAC-A
• MyVariant Identifiers: chr16:g.11647568_11647569del (hg19) ; chr16:g.11553712_11553713del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11553715_11553716del , CM000678.2:g.11553715_11553716del	GRCh38
NC_000016.9:g.11647571_11647572del , CM000678.1:g.11647571_11647572del	GRCh37
NC_000016.8:g.11555072_11555073del	NCBI36
NG_009008.1:g.38238_38239del , LRG_253:g.38238_38239del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622633.5:c.221-24_221-23del MANE Select	ENSP00000483114.1:n.221-24_221-23del
ENST00000339430.9:c.221-24_221-23del	ENSP00000340118.5:n.221-24_221-23del
ENST00000381810.7:c.221-24_221-23del	ENSP00000371231.3:n.221-24_221-23del
ENST00000413364.6:c.221-24_221-23del	ENSP00000397958.2:n.221-24_221-23del
ENST00000570798.5:c.221-24_221-23del	ENSP00000458871.1:n.221-24_221-23del
ENST00000570904.5:c.221-24_221-23del	ENSP00000459138.1:n.221-24_221-23del
ENST00000571459.5:c.220+2798_220+2799del	ENSP00000459603.1:n.220+2798_220+2799del
ENST00000571627.5:c.221-24_221-23del	ENSP00000460743.1:n.221-24_221-23del
ENST00000571688.5:c.221-24_221-23del	ENSP00000459533.1:n.221-24_221-23del
ENST00000571976.1:c.221-24_221-23del	ENSP00000460133.1:n.221-24_221-23del
ENST00000572255.5:c.-59-24_-59-23del	ENSP00000458836.1:n.-59-24_-59-23del
ENST00000573332.5:c.*10_*11del	ENSP00000460873.1:n.*10_*11del
ENST00000574701.5:c.221-24_221-23del	ENSP00000458981.1:n.221-24_221-23del
ENST00000574763.5:c.221-24_221-23del	ENSP00000461813.1:n.221-24_221-23del
ENST00000575426.1:c.40-24_40-23del
ENST00000576036.5:c.221-24_221-23del	ENSP00000461667.1:n.221-24_221-23del
ENST00000620789.4:c.221-24_221-23del	ENSP00000481589.1:n.221-24_221-23del
ENST00000622633.4:c.221-24_221-23del	ENSP00000483114.1:n.221-24_221-23del
NM_001136472.1:c.221-24_221-23del	NP_001129944.1:n.221-24_221-23del
NM_001136473.1:c.221-24_221-23del , LRG_253t1:c.221-24_221-23del	NP_001129945.1:n.221-24_221-23del
NM_004862.3:c.221-24_221-23del	NP_004853.2:n.221-24_221-23del
NR_024320.1:n.355-24_355-23del
XM_006720982.2:c.221-24_221-23del	XP_006721045.1:n.221-24_221-23del
XM_006720983.2:c.221-24_221-23del	XP_006721046.1:n.221-24_221-23del
XM_006720984.2:c.221-24_221-23del	XP_006721047.1:n.221-24_221-23del
XM_006720985.2:c.221-24_221-23del	XP_006721048.1:n.221-24_221-23del
XM_011522754.1:c.311-24_311-23del	XP_011521056.1:n.311-24_311-23del
XM_006720982.3:c.221-24_221-23del	XP_006721045.1:n.221-24_221-23del
XM_006720983.4:c.221-24_221-23del	XP_006721046.1:n.221-24_221-23del
XM_006720984.4:c.221-24_221-23del	XP_006721047.1:n.221-24_221-23del
XM_006720985.3:c.221-24_221-23del	XP_006721048.1:n.221-24_221-23del
XM_011522754.3:c.311-24_311-23del	XP_011521056.1:n.311-24_311-23del
XM_017023896.1:c.221-24_221-23del	XP_016879385.1:n.221-24_221-23del
NM_001136472.2:c.221-24_221-23del MANE Select	NP_001129944.1:n.221-24_221-23del
NM_004862.4:c.221-24_221-23del	NP_004853.2:n.221-24_221-23del
NR_024320.2:n.355-24_355-23del