Canonical Allele Identifier: CA492065371

Gene: FANCI

Linked Data

• MyVariant Identifiers: chr15:g.89807224T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89263993T>G , CM000677.2:g.89263993T>G	GRCh38
NC_000015.9:g.89807224T>G , CM000677.1:g.89807224T>G	GRCh37
NC_000015.8:g.87608228T>G	NCBI36
NG_011736.1:g.25031T>G , LRG_500:g.25031T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696717.1:c.357T>G	ENSP00000512830.1:p.Pro119=
ENST00000696718.1:c.99T>G	ENSP00000512831.1:p.Pro33=
ENST00000696719.1:c.636T>G	ENSP00000512832.1:p.Pro212=
ENST00000310775.12:c.636T>G MANE Select	ENSP00000310842.8:p.Pro212=
ENST00000674831.1:c.636T>G	ENSP00000502474.1:p.Pro212=
ENST00000676003.1:c.636T>G	ENSP00000502254.1:p.Pro212=
ENST00000300027.12:c.636T>G	ENSP00000300027.8:p.Pro212=
ENST00000310775.11:c.636T>G	ENSP00000310842.7:p.Pro212=
ENST00000447611.6:c.636T>G	ENSP00000413249.2:p.Pro212=
ENST00000561894.1:c.115T>G
ENST00000563250.5:c.636T>G	ENSP00000457029.1:p.Pro212=
ENST00000565255.5:c.636T>G	ENSP00000454371.1:p.Pro212=
ENST00000565522.5:n.129+16267T>G
ENST00000567996.5:c.636T>G	ENSP00000458024.1:p.Pro212=
ENST00000570225.5:c.174T>G	ENSP00000454669.1:p.Pro58=
NM_001113378.1:c.636T>G , LRG_500t1:c.636T>G	NP_001106849.1:p.Pro212=
NM_018193.2:c.636T>G	NP_060663.2:p.Pro212=
XM_011521756.1:c.636T>G	XP_011520058.1:p.Pro212=
XM_011521757.1:c.636T>G	XP_011520059.1:p.Pro212=
XM_011521758.1:c.636T>G	XP_011520060.1:p.Pro212=
XM_011521759.1:c.636T>G	XP_011520061.1:p.Pro212=
XM_011521760.1:c.636T>G	XP_011520062.1:p.Pro212=
XM_011521761.1:c.636T>G	XP_011520063.1:p.Pro212=
XM_011521762.1:c.636T>G	XP_011520064.1:p.Pro212=
XM_011521763.1:c.636T>G	XP_011520065.1:p.Pro212=
XM_011521764.1:c.636T>G	XP_011520066.1:p.Pro212=
XM_011521765.1:c.357T>G	XP_011520067.1:p.Pro119=
XM_011521766.1:c.357T>G	XP_011520068.1:p.Pro119=
XM_011521767.1:c.357T>G	XP_011520069.1:p.Pro119=
XM_011521768.1:c.636T>G	XP_011520070.1:p.Pro212=
XM_011521769.1:c.636T>G	XP_011520071.1:p.Pro212=
XM_011521756.2:c.636T>G	XP_011520058.1:p.Pro212=
XM_011521757.2:c.636T>G	XP_011520059.1:p.Pro212=
XM_011521764.2:c.636T>G	XP_011520066.1:p.Pro212=
XM_011521767.2:c.357T>G	XP_011520069.1:p.Pro119=
NM_001113378.2:c.636T>G MANE Select	NP_001106849.1:p.Pro212=
NM_001376910.1:c.357T>G	NP_001363839.1:p.Pro119=
NM_001376911.1:c.636T>G	NP_001363840.1:p.Pro212=
NM_018193.3:c.636T>G	NP_060663.2:p.Pro212=