Canonical Allele Identifier: CA397483845

Gene: FANCA ZNF276

Linked Data

• dbSNP Id: rs2151710946
• MyVariant Identifiers: chr16:g.89805380G>A (hg19) ; chr16:g.89738972G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89738972G>A , CM000678.2:g.89738972G>A	GRCh38
NC_000016.9:g.89805380G>A , CM000678.1:g.89805380G>A	GRCh37
NC_000016.8:g.88332881G>A	NCBI36
NG_011706.1:g.82686C>T , LRG_495:g.82686C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*2743C>T (FANCA)	ENSP00000512522.1:n.*2743C>T
ENST00000564475.6:c.4174C>T (FANCA)	ENSP00000454977.2:p.Gln1392Ter
ENST00000567510.2:c.2744C>T (FANCA)	ENSP00000455969.1:n.2744C>T
ENST00000568369.6:c.4174C>T (FANCA)	ENSP00000456829.1:p.Gln1392Ter
ENST00000696274.1:n.4131C>T (FANCA)
ENST00000696275.1:c.*3409C>T (FANCA)	ENSP00000512517.1:n.*3409C>T
ENST00000696286.1:c.*83C>T (FANCA)	ENSP00000512523.1:n.*83C>T
ENST00000696287.1:c.4045C>T (FANCA)	ENSP00000512524.1:p.Gln1349Ter
ENST00000696291.1:c.*3602C>T (FANCA)	ENSP00000512530.1:n.*3602C>T
ENST00000389301.8:c.4170C>T (FANCA) MANE Select	ENSP00000373952.3:p.Gly1390=
ENST00000443381.7:c.*726G>A (ZNF276) MANE Select	ENSP00000415836.2:n.*726G>A
ENST00000289816.9:c.*726G>A (ZNF276)	ENSP00000289816.5:n.*726G>A
ENST00000389301.7:c.4170C>T (FANCA)	ENSP00000373952.3:p.Gly1390=
ENST00000561722.5:c.435+44C>T (FANCA)	ENSP00000456608.1:n.435+44C>T
ENST00000562424.1:n.441C>T (FANCA)
ENST00000563983.5:n.2559G>A (ZNF276)
ENST00000564475.5:c.504C>T (FANCA)
ENST00000564870.1:c.371C>T (FANCA)
ENST00000567879.5:c.544C>T (FANCA)	ENSP00000457006.1:p.Gln182Ter
ENST00000568369.5:c.4174C>T (FANCA)	ENSP00000456829.1:p.Gln1392Ter
NM_000135.2:c.4170C>T , LRG_495t1:c.4170C>T (FANCA)	NP_000126.2:p.Gly1390=
NM_001113525.1:c.*726G>A (ZNF276)	NP_001106997.1:n.*726G>A
NM_001286167.1:c.4174C>T (FANCA)	NP_001273096.1:p.Gln1392Ter
NM_152287.3:c.*726G>A (ZNF276)	NP_689500.2:n.*726G>A
NR_110122.1:n.2743G>A (ZNF276)
NR_110126.1:n.2626G>A (ZNF276)
NR_110128.1:n.2549G>A (ZNF276)
NR_110129.1:n.2638G>A (ZNF276)
XM_005256294.3:c.4174C>T (FANCA)	XP_005256351.1:p.Gln1392Ter
XM_011522945.1:c.4045C>T (FANCA)	XP_011521247.1:p.Gln1349Ter
XM_011522946.1:c.3151C>T (FANCA)	XP_011521248.1:p.Gln1051Ter
XM_011522947.1:c.3151C>T (FANCA)	XP_011521249.1:p.Gln1051Ter
XR_933244.1:n.4137C>T (FANCA)
XR_933245.1:n.4074C>T (FANCA)
NM_000135.3:c.4170C>T (FANCA)	NP_000126.2:p.Gly1390=
NM_001286167.2:c.4174C>T (FANCA)	NP_001273096.1:p.Gln1392Ter
XM_005256294.4:c.4174C>T (FANCA)	XP_005256351.1:p.Gln1392Ter
XM_011522945.2:c.4045C>T (FANCA)	XP_011521247.1:p.Gln1349Ter
XM_011522946.3:c.3151C>T (FANCA)	XP_011521248.1:p.Gln1051Ter
XM_011522947.2:c.3151C>T (FANCA)	XP_011521249.1:p.Gln1051Ter
XM_017023044.2:c.4041C>T (FANCA)	XP_016878533.1:p.Gly1347=
XM_017023890.1:c.*726G>A (ZNF276)	XP_016879379.1:n.*726G>A
XM_024450189.1:c.3151C>T (FANCA)	XP_024305957.1:p.Gln1051Ter
XR_933244.2:n.4137C>T (FANCA)
XR_933245.2:n.4074C>T (FANCA)
XR_933484.2:n.2737G>A (ZNF276)
NM_000135.4:c.4170C>T (FANCA) MANE Select	NP_000126.2:p.Gly1390=
NM_001113525.2:c.*726G>A (ZNF276) MANE Select	NP_001106997.1:n.*726G>A
NM_001286167.3:c.4174C>T (FANCA)	NP_001273096.1:p.Gln1392Ter
NM_152287.4:c.*726G>A (ZNF276)	NP_689500.2:n.*726G>A
NR_110122.2:n.2726G>A (ZNF276)
NR_110126.2:n.2609G>A (ZNF276)
NR_110129.2:n.2643G>A (ZNF276)
NR_110128.2:n.2549G>A (ZNF276)