Canonical Allele Identifier: CA912996776

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805582_89805584del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739174_89739176del , CM000678.2:g.89739174_89739176del	GRCh38
NC_000016.9:g.89805582_89805584del , CM000678.1:g.89805582_89805584del	GRCh37
NC_000016.8:g.88333083_88333085del	NCBI36
NG_011706.1:g.82482_82484del , LRG_495:g.82482_82484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2697_*2699del (FANCA)	ENSP00000512522.1:n.*2697_*2699del
ENST00000564475.6:c.4124_4126del (FANCA)	ENSP00000454977.2:p.Thr1375_Val1376delinsIle
ENST00000567510.2:c.2694_2696del (FANCA)	ENSP00000455969.1:n.2694_2696del
ENST00000568369.6:c.4124_4126del (FANCA)	ENSP00000456829.1:p.Thr1375_Val1376delinsIle
ENST00000696274.1:n.4085_4087del (FANCA)
ENST00000696275.1:c.*3359_*3361del (FANCA)	ENSP00000512517.1:n.*3359_*3361del
ENST00000696286.1:c.*37_*39del (FANCA)	ENSP00000512523.1:n.*37_*39del
ENST00000696287.1:c.3995_3997del (FANCA)	ENSP00000512524.1:p.Thr1332_Val1333delinsIle
ENST00000696291.1:c.*3556_*3558del (FANCA)	ENSP00000512530.1:n.*3556_*3558del
ENST00000389301.8:c.4124_4126del (FANCA) MANE Select	ENSP00000373952.3:p.Thr1375_Val1376delinsIle
ENST00000443381.7:c.*928_*930del (ZNF276) MANE Select	ENSP00000415836.2:n.*928_*930del
ENST00000289816.9:c.*928_*930del (ZNF276)	ENSP00000289816.5:n.*928_*930del
ENST00000389301.7:c.4124_4126del (FANCA)	ENSP00000373952.3:p.Thr1375_Val1376delinsIle
ENST00000561722.5:c.275_277del (FANCA)	ENSP00000456608.1:p.Thr92_Val93delinsIle
ENST00000562424.1:n.395_397del (FANCA)
ENST00000563983.5:n.2761_2763del (ZNF276)
ENST00000564475.5:c.454_456del (FANCA)
ENST00000564870.1:c.325_327del (FANCA)
ENST00000567879.5:c.503_505del (FANCA)	ENSP00000457006.1:p.Thr168_Val169delinsIle
ENST00000568369.5:c.4124_4126del (FANCA)	ENSP00000456829.1:p.Thr1375_Val1376delinsIle
NM_000135.2:c.4124_4126del , LRG_495t1:c.4124_4126del (FANCA)	NP_000126.2:p.Thr1375_Val1376delinsIle
NM_001113525.1:c.*928_*930del (ZNF276)	NP_001106997.1:n.*928_*930del
NM_001286167.1:c.4124_4126del (FANCA)	NP_001273096.1:p.Thr1375_Val1376delinsIle
NM_152287.3:c.*928_*930del (ZNF276)	NP_689500.2:n.*928_*930del
NR_110122.1:n.2945_2947del (ZNF276)
NR_110126.1:n.2828_2830del (ZNF276)
NR_110128.1:n.2751_2753del (ZNF276)
NR_110129.1:n.2840_2842del (ZNF276)
XM_005256294.3:c.4124_4126del (FANCA)	XP_005256351.1:p.Thr1375_Val1376delinsIle
XM_011522945.1:c.3995_3997del (FANCA)	XP_011521247.1:p.Thr1332_Val1333delinsIle
XM_011522946.1:c.3101_3103del (FANCA)	XP_011521248.1:p.Thr1034_Val1035delinsIle
XM_011522947.1:c.3101_3103del (FANCA)	XP_011521249.1:p.Thr1034_Val1035delinsIle
XR_933244.1:n.4091_4093del (FANCA)
XR_933245.1:n.4028_4030del (FANCA)
NM_000135.3:c.4124_4126del (FANCA)	NP_000126.2:p.Thr1375_Val1376delinsIle
NM_001286167.2:c.4124_4126del (FANCA)	NP_001273096.1:p.Thr1375_Val1376delinsIle
XM_005256294.4:c.4124_4126del (FANCA)	XP_005256351.1:p.Thr1375_Val1376delinsIle
XM_011522945.2:c.3995_3997del (FANCA)	XP_011521247.1:p.Thr1332_Val1333delinsIle
XM_011522946.3:c.3101_3103del (FANCA)	XP_011521248.1:p.Thr1034_Val1035delinsIle
XM_011522947.2:c.3101_3103del (FANCA)	XP_011521249.1:p.Thr1034_Val1035delinsIle
XM_017023044.2:c.3995_3997del (FANCA)	XP_016878533.1:p.Thr1332_Val1333delinsIle
XM_017023890.1:c.*928_*930del (ZNF276)	XP_016879379.1:n.*928_*930del
XM_024450189.1:c.3101_3103del (FANCA)	XP_024305957.1:p.Thr1034_Val1035delinsIle
XR_933244.2:n.4091_4093del (FANCA)
XR_933245.2:n.4028_4030del (FANCA)
XR_933484.2:n.2939_2941del (ZNF276)
NM_000135.4:c.4124_4126del (FANCA) MANE Select	NP_000126.2:p.Thr1375_Val1376delinsIle
NM_001113525.2:c.*928_*930del (ZNF276) MANE Select	NP_001106997.1:n.*928_*930del
NM_001286167.3:c.4124_4126del (FANCA)	NP_001273096.1:p.Thr1375_Val1376delinsIle
NM_152287.4:c.*928_*930del (ZNF276)	NP_689500.2:n.*928_*930del
NR_110122.2:n.2928_2930del (ZNF276)
NR_110126.2:n.2811_2813del (ZNF276)
NR_110129.2:n.2845_2847del (ZNF276)
NR_110128.2:n.2751_2753del (ZNF276)