Canonical Allele Identifier: CA397484325

Gene: FANCA ZNF276

Linked Data

• MyVariant Identifiers: chr16:g.89805579A>C (hg19) ; chr16:g.89739171A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89739171A>C , CM000678.2:g.89739171A>C	GRCh38
NC_000016.9:g.89805579A>C , CM000678.1:g.89805579A>C	GRCh37
NC_000016.8:g.88333080A>C	NCBI36
NG_011706.1:g.82487T>G , LRG_495:g.82487T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2702T>G (FANCA)	ENSP00000512522.1:n.*2702T>G
ENST00000564475.6:c.4129T>G (FANCA)	ENSP00000454977.2:p.Ser1377Ala
ENST00000567510.2:c.2699T>G (FANCA)	ENSP00000455969.1:n.2699T>G
ENST00000568369.6:c.4129T>G (FANCA)	ENSP00000456829.1:p.Ser1377Ala
ENST00000696274.1:n.4090T>G (FANCA)
ENST00000696275.1:c.*3364T>G (FANCA)	ENSP00000512517.1:n.*3364T>G
ENST00000696286.1:c.*42T>G (FANCA)	ENSP00000512523.1:n.*42T>G
ENST00000696287.1:c.4000T>G (FANCA)	ENSP00000512524.1:p.Ser1334Ala
ENST00000696291.1:c.*3561T>G (FANCA)	ENSP00000512530.1:n.*3561T>G
ENST00000389301.8:c.4129T>G (FANCA) MANE Select	ENSP00000373952.3:p.Ser1377Ala
ENST00000443381.7:c.*925A>C (ZNF276) MANE Select	ENSP00000415836.2:n.*925A>C
ENST00000289816.9:c.*925A>C (ZNF276)	ENSP00000289816.5:n.*925A>C
ENST00000389301.7:c.4129T>G (FANCA)	ENSP00000373952.3:p.Ser1377Ala
ENST00000561722.5:c.280T>G (FANCA)	ENSP00000456608.1:p.Ser94Ala
ENST00000562424.1:n.400T>G (FANCA)
ENST00000563983.5:n.2758A>C (ZNF276)
ENST00000564475.5:c.459T>G (FANCA)
ENST00000564870.1:c.330T>G (FANCA)
ENST00000567879.5:c.508T>G (FANCA)	ENSP00000457006.1:p.Ser170Ala
ENST00000568369.5:c.4129T>G (FANCA)	ENSP00000456829.1:p.Ser1377Ala
NM_000135.2:c.4129T>G , LRG_495t1:c.4129T>G (FANCA)	NP_000126.2:p.Ser1377Ala
NM_001113525.1:c.*925A>C (ZNF276)	NP_001106997.1:n.*925A>C
NM_001286167.1:c.4129T>G (FANCA)	NP_001273096.1:p.Ser1377Ala
NM_152287.3:c.*925A>C (ZNF276)	NP_689500.2:n.*925A>C
NR_110122.1:n.2942A>C (ZNF276)
NR_110126.1:n.2825A>C (ZNF276)
NR_110128.1:n.2748A>C (ZNF276)
NR_110129.1:n.2837A>C (ZNF276)
XM_005256294.3:c.4129T>G (FANCA)	XP_005256351.1:p.Ser1377Ala
XM_011522945.1:c.4000T>G (FANCA)	XP_011521247.1:p.Ser1334Ala
XM_011522946.1:c.3106T>G (FANCA)	XP_011521248.1:p.Ser1036Ala
XM_011522947.1:c.3106T>G (FANCA)	XP_011521249.1:p.Ser1036Ala
XR_933244.1:n.4096T>G (FANCA)
XR_933245.1:n.4033T>G (FANCA)
NM_000135.3:c.4129T>G (FANCA)	NP_000126.2:p.Ser1377Ala
NM_001286167.2:c.4129T>G (FANCA)	NP_001273096.1:p.Ser1377Ala
XM_005256294.4:c.4129T>G (FANCA)	XP_005256351.1:p.Ser1377Ala
XM_011522945.2:c.4000T>G (FANCA)	XP_011521247.1:p.Ser1334Ala
XM_011522946.3:c.3106T>G (FANCA)	XP_011521248.1:p.Ser1036Ala
XM_011522947.2:c.3106T>G (FANCA)	XP_011521249.1:p.Ser1036Ala
XM_017023044.2:c.4000T>G (FANCA)	XP_016878533.1:p.Ser1334Ala
XM_017023890.1:c.*925A>C (ZNF276)	XP_016879379.1:n.*925A>C
XM_024450189.1:c.3106T>G (FANCA)	XP_024305957.1:p.Ser1036Ala
XR_933244.2:n.4096T>G (FANCA)
XR_933245.2:n.4033T>G (FANCA)
XR_933484.2:n.2936A>C (ZNF276)
NM_000135.4:c.4129T>G (FANCA) MANE Select	NP_000126.2:p.Ser1377Ala
NM_001113525.2:c.*925A>C (ZNF276) MANE Select	NP_001106997.1:n.*925A>C
NM_001286167.3:c.4129T>G (FANCA)	NP_001273096.1:p.Ser1377Ala
NM_152287.4:c.*925A>C (ZNF276)	NP_689500.2:n.*925A>C
NR_110122.2:n.2925A>C (ZNF276)
NR_110126.2:n.2808A>C (ZNF276)
NR_110129.2:n.2842A>C (ZNF276)
NR_110128.2:n.2748A>C (ZNF276)