Canonical Allele Identifier: CA2207696430

Gene: LITAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11553392_11553406delinsCAGAACCAGATTCCA , CM000678.2:g.11553392_11553406delinsCAGAACCAGATTCCA	GRCh38
NC_000016.9:g.11647248_11647262delinsCAGAACCAGATTCCA , CM000678.1:g.11647248_11647262delinsCAGAACCAGATTCCA	GRCh37
NC_000016.8:g.11554749_11554763delinsCAGAACCAGATTCCA	NCBI36
NG_009008.1:g.38545_38559delinsTGGAATCTGGTTCTG , LRG_253:g.38545_38559delinsTGGAATCTGGTTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622633.5:c.377+127_377+141delinsTGGAATCTGGTTCTG MANE Select	ENSP00000483114.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000339430.9:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000340118.5:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000381810.7:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000371231.3:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000413364.6:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000397958.2:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000570798.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000458871.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000570904.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000459138.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000571459.5:c.220+3105_220+3119delinsTGGAATCTGGTTCTG	ENSP00000459603.1:n.220+3105_220+3119delinsTGGAATCTGGTTCTG
ENST00000571627.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000460743.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000571688.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000459533.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000572255.5:c.98+127_98+141delinsTGGAATCTGGTTCTG	ENSP00000458836.1:n.98+127_98+141delinsTGGAATCTGGTTCTG
ENST00000573332.5:c.*190+127_*190+141delinsTGGAATCTGGTTCTG	ENSP00000460873.1:n.*190+127_*190+141delinsTGGAATCTGGTTCTG
ENST00000574701.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000458981.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000574763.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000461813.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000575426.1:c.196+127_196+141delinsTGGAATCTGGTTCTG
ENST00000576036.5:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000461667.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000620789.4:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000481589.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
ENST00000622633.4:c.377+127_377+141delinsTGGAATCTGGTTCTG	ENSP00000483114.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
NM_001136472.1:c.377+127_377+141delinsTGGAATCTGGTTCTG	NP_001129944.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
NM_001136473.1:c.377+127_377+141delinsTGGAATCTGGTTCTG , LRG_253t1:c.377+127_377+141delinsTGGAATCTGGTTCTG	NP_001129945.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
NM_004862.3:c.377+127_377+141delinsTGGAATCTGGTTCTG	NP_004853.2:n.377+127_377+141delinsTGGAATCTGGTTCTG
NR_024320.1:n.511+127_511+141delinsTGGAATCTGGTTCTG
XM_006720982.2:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721045.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_006720983.2:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721046.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_006720984.2:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721047.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_006720985.2:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721048.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_011522754.1:c.467+127_467+141delinsTGGAATCTGGTTCTG	XP_011521056.1:n.467+127_467+141delinsTGGAATCTGGTTCTG
XM_006720982.3:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721045.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_006720983.4:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721046.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_006720984.4:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721047.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_006720985.3:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_006721048.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
XM_011522754.3:c.467+127_467+141delinsTGGAATCTGGTTCTG	XP_011521056.1:n.467+127_467+141delinsTGGAATCTGGTTCTG
XM_017023896.1:c.377+127_377+141delinsTGGAATCTGGTTCTG	XP_016879385.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
NM_001136472.2:c.377+127_377+141delinsTGGAATCTGGTTCTG MANE Select	NP_001129944.1:n.377+127_377+141delinsTGGAATCTGGTTCTG
NM_004862.4:c.377+127_377+141delinsTGGAATCTGGTTCTG	NP_004853.2:n.377+127_377+141delinsTGGAATCTGGTTCTG
NR_024320.2:n.511+127_511+141delinsTGGAATCTGGTTCTG