Canonical Allele Identifier: CA497195052

Gene: FANCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89742926A>G , CM000678.2:g.89742926A>G	GRCh38
NC_000016.9:g.89809334A>G , CM000678.1:g.89809334A>G	GRCh37
NC_000016.8:g.88336835A>G	NCBI36
NG_011706.1:g.78732T>C , LRG_495:g.78732T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000135.4:c.3639T>C MANE Select	NP_000126.2:p.Pro1213=
ENST00000389301.8:c.3639T>C MANE Select	ENSP00000373952.3:p.Pro1213=
NM_000135.2:c.3639T>C , LRG_495t1:c.3639T>C	NP_000126.2:p.Pro1213=
NM_000135.3:c.3639T>C	NP_000126.2:p.Pro1213=
NM_001286167.1:c.3639T>C	NP_001273096.1:p.Pro1213=
NM_001286167.2:c.3639T>C	NP_001273096.1:p.Pro1213=
NM_001286167.3:c.3639T>C	NP_001273096.1:p.Pro1213=
ENST00000305699.15:n.882T>C
ENST00000389301.7:c.3639T>C	ENSP00000373952.3:p.Pro1213=
ENST00000561667.2:c.*2117T>C	ENSP00000512522.1:n.*2117T>C
ENST00000564475.6:c.3639T>C	ENSP00000454977.2:p.Pro1213=
ENST00000564969.5:n.50+2033T>C
ENST00000567510.2:c.2209T>C	ENSP00000455969.1:n.2209T>C
ENST00000567879.5:c.117T>C	ENSP00000457006.1:p.Pro39=
ENST00000567988.5:c.891T>C
ENST00000568369.5:c.3639T>C	ENSP00000456829.1:p.Pro1213=
ENST00000568369.6:c.3639T>C	ENSP00000456829.1:p.Pro1213=
ENST00000568626.1:c.474+2033T>C
ENST00000696274.1:n.3600T>C
ENST00000696275.1:c.*2874T>C	ENSP00000512517.1:n.*2874T>C
ENST00000696286.1:c.3639T>C	ENSP00000512523.1:p.Pro1213=
ENST00000696287.1:c.3510T>C	ENSP00000512524.1:p.Pro1170=
ENST00000696291.1:c.*3071T>C	ENSP00000512530.1:n.*3071T>C
XM_005256294.3:c.3639T>C	XP_005256351.1:p.Pro1213=
XM_005256294.4:c.3639T>C	XP_005256351.1:p.Pro1213=
XM_011522945.1:c.3510T>C	XP_011521247.1:p.Pro1170=
XM_011522945.2:c.3510T>C	XP_011521247.1:p.Pro1170=
XM_011522946.1:c.2616T>C	XP_011521248.1:p.Pro872=
XM_011522946.3:c.2616T>C	XP_011521248.1:p.Pro872=
XM_011522947.1:c.2616T>C	XP_011521249.1:p.Pro872=
XM_011522947.2:c.2616T>C	XP_011521249.1:p.Pro872=
XM_017023044.2:c.3510T>C	XP_016878533.1:p.Pro1170=
XM_024450189.1:c.2616T>C	XP_024305957.1:p.Pro872=
XR_001751866.1:n.3509T>C
XR_933244.1:n.3682T>C
XR_933244.2:n.3682T>C
XR_933245.1:n.3669+2033T>C
XR_933245.2:n.3669+2033T>C
XR_933246.1:n.3509T>C