Canonical Allele Identifier: CA397485115

Gene: FANCA ZNF276

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89740100C>G , CM000678.2:g.89740100C>G	GRCh38
NC_000016.9:g.89806508C>G , CM000678.1:g.89806508C>G	GRCh37
NC_000016.8:g.88334009C>G	NCBI36
NG_011706.1:g.81558G>C , LRG_495:g.81558G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.3829-1G>C (FANCA) MANE Select	NP_000126.2:n.3829-1G>C
NM_001113525.2:c.*1854C>G (ZNF276) MANE Select	NP_001106997.1:n.*1854C>G
ENST00000389301.8:c.3829-1G>C (FANCA) MANE Select	ENSP00000373952.3:n.3829-1G>C
ENST00000443381.7:c.*1854C>G (ZNF276) MANE Select	ENSP00000415836.2:n.*1854C>G
NM_000135.2:c.3829-1G>C , LRG_495t1:c.3829-1G>C (FANCA)	NP_000126.2:n.3829-1G>C
NM_000135.3:c.3829-1G>C (FANCA)	NP_000126.2:n.3829-1G>C
NM_001113525.1:c.*1854C>G (ZNF276)	NP_001106997.1:n.*1854C>G
NM_001286167.1:c.3829-1G>C (FANCA)	NP_001273096.1:n.3829-1G>C
NM_001286167.2:c.3829-1G>C (FANCA)	NP_001273096.1:n.3829-1G>C
NM_001286167.3:c.3829-1G>C (FANCA)	NP_001273096.1:n.3829-1G>C
NM_152287.3:c.*1854C>G (ZNF276)	NP_689500.2:n.*1854C>G
NM_152287.4:c.*1854C>G (ZNF276)	NP_689500.2:n.*1854C>G
NR_110122.2:n.3854C>G (ZNF276)
NR_110126.2:n.3737C>G (ZNF276)
NR_110128.2:n.3677C>G (ZNF276)
NR_110129.2:n.3771C>G (ZNF276)
ENST00000289816.9:c.*1854C>G (ZNF276)	ENSP00000289816.5:n.*1854C>G
ENST00000305699.15:n.1072-1G>C (FANCA)
ENST00000389301.7:c.3829-1G>C (FANCA)	ENSP00000373952.3:n.3829-1G>C
ENST00000561667.2:c.*2307-1G>C (FANCA)	ENSP00000512522.1:n.*2307-1G>C
ENST00000564475.5:c.159-1G>C (FANCA)
ENST00000564475.6:c.3829-1G>C (FANCA)	ENSP00000454977.2:n.3829-1G>C
ENST00000564870.1:c.30-1G>C (FANCA)
ENST00000564969.5:n.114-1G>C (FANCA)
ENST00000567510.2:c.2399-1G>C (FANCA)	ENSP00000455969.1:n.2399-1G>C
ENST00000567879.5:c.307-1G>C (FANCA)	ENSP00000457006.1:n.307-1G>C
ENST00000568369.5:c.3829-1G>C (FANCA)	ENSP00000456829.1:n.3829-1G>C
ENST00000568369.6:c.3829-1G>C (FANCA)	ENSP00000456829.1:n.3829-1G>C
ENST00000568626.1:c.538-1G>C (FANCA)
ENST00000696274.1:n.3790-1G>C (FANCA)
ENST00000696275.1:c.*3064-1G>C (FANCA)	ENSP00000512517.1:n.*3064-1G>C
ENST00000696286.1:c.3829-1G>C (FANCA)	ENSP00000512523.1:n.3829-1G>C
ENST00000696287.1:c.3700-1G>C (FANCA)	ENSP00000512524.1:n.3700-1G>C
ENST00000696291.1:c.*3261-1G>C (FANCA)	ENSP00000512530.1:n.*3261-1G>C
XM_005256294.3:c.3829-1G>C (FANCA)	XP_005256351.1:n.3829-1G>C
XM_005256294.4:c.3829-1G>C (FANCA)	XP_005256351.1:n.3829-1G>C
XM_011522945.1:c.3700-1G>C (FANCA)	XP_011521247.1:n.3700-1G>C
XM_011522945.2:c.3700-1G>C (FANCA)	XP_011521247.1:n.3700-1G>C
XM_011522946.1:c.2806-1G>C (FANCA)	XP_011521248.1:n.2806-1G>C
XM_011522946.3:c.2806-1G>C (FANCA)	XP_011521248.1:n.2806-1G>C
XM_011522947.1:c.2806-1G>C (FANCA)	XP_011521249.1:n.2806-1G>C
XM_011522947.2:c.2806-1G>C (FANCA)	XP_011521249.1:n.2806-1G>C
XM_017023044.2:c.3700-1G>C (FANCA)	XP_016878533.1:n.3700-1G>C
XM_024450189.1:c.2806-1G>C (FANCA)	XP_024305957.1:n.2806-1G>C
XR_001751866.1:n.3699-1G>C (FANCA)
XR_933244.1:n.3872-1G>C (FANCA)
XR_933244.2:n.3872-1G>C (FANCA)
XR_933245.1:n.3733-1G>C (FANCA)
XR_933245.2:n.3733-1G>C (FANCA)
XR_933246.1:n.3699-1G>C (FANCA)