Canonical Allele Identifier: CA2805167449

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89316864_89316865insGTC , CM000677.2:g.89316864_89316865insGTC GRCh38
NC_000015.9:g.89860095_89860096insGTC , CM000677.1:g.89860095_89860096insGTC GRCh37
NC_000015.8:g.87661099_87661100insGTC NCBI36
NG_008218.1:g.22931_22932insGAC
NG_011736.1:g.77902_77903insGTC , LRG_500:g.77902_77903insGTC
NG_008218.2:g.22931_22932insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3644-38_3644-37insGAC (POLG) ENSP00000516154.1:n.3644-38_3644-37insGAC
ENST00000696717.1:c.*405_*406insGTC (FANCI) ENSP00000512830.1:n.*405_*406insGTC
ENST00000696718.1:c.*405_*406insGTC (FANCI) ENSP00000512831.1:n.*405_*406insGTC
ENST00000696719.1:c.*405_*406insGTC (FANCI) ENSP00000512832.1:n.*405_*406insGTC
ENST00000268124.11:c.3644-38_3644-37insGAC (POLG) MANE Select ENSP00000268124.5:n.3644-38_3644-37insGAC
ENST00000310775.12:c.*405_*406insGTC (FANCI) MANE Select ENSP00000310842.8:n.*405_*406insGTC
ENST00000530292.3:c.3344-38_3344-37insGAC (POLG) ENSP00000432885.2:n.3344-38_3344-37insGAC
ENST00000635986.2:c.*714-38_*714-37insGAC (POLG) ENSP00000490653.2:n.*714-38_*714-37insGAC
ENST00000636774.1:c.*2248-38_*2248-37insGAC (POLG) ENSP00000489799.1:n.*2248-38_*2248-37insGAC
ENST00000637238.1:c.2552-38_2552-37insGAC (POLG) ENSP00000490756.1:n.2552-38_2552-37insGAC
ENST00000637264.1:c.2656-38_2656-37insGAC (POLG)
ENST00000666746.1:c.3221-38_3221-37insGAC (POLG)
ENST00000672071.1:n.4846-38_4846-37insGAC (POLG)
ENST00000672695.1:n.1423-38_1423-37insGAC (POLG)
ENST00000672923.2:n.3644-38_3644-37insGAC (POLG)
ENST00000675352.1:n.3597_3598insGTC (FANCI)
ENST00000676110.1:n.3973_3974insGTC (FANCI)
ENST00000268124.9:c.3644-38_3644-37insGAC (POLG) ENSP00000268124.5:n.3644-38_3644-37insGAC
ENST00000300027.12:c.*405_*406insGTC (FANCI) ENSP00000300027.8:n.*405_*406insGTC
ENST00000310775.11:c.*405_*406insGTC (FANCI) ENSP00000310842.7:n.*405_*406insGTC
ENST00000442287.6:c.3644-38_3644-37insGAC (POLG) ENSP00000399851.2:n.3644-38_3644-37insGAC
ENST00000526671.1:n.454-38_454-37insGAC (POLG)
ENST00000530292.2:c.827-38_827-37insGAC (POLG) ENSP00000432885.1:n.827-38_827-37insGAC
ENST00000566895.5:n.4399_4400insGTC (FANCI)
ENST00000631044.2:c.*3068-38_*3068-37insGAC (POLG) ENSP00000486730.1:n.*3068-38_*3068-37insGAC
NM_001113378.1:c.*405_*406insGTC , LRG_500t1:c.*405_*406insGTC (FANCI) NP_001106849.1:n.*405_*406insGTC
NM_001126131.1:c.3644-38_3644-37insGAC (POLG) NP_001119603.1:n.3644-38_3644-37insGAC
NM_002693.2:c.3644-38_3644-37insGAC (POLG) NP_002684.1:n.3644-38_3644-37insGAC
NM_018193.2:c.*405_*406insGTC (FANCI) NP_060663.2:n.*405_*406insGTC
XM_011521756.1:c.*405_*406insGTC (FANCI) XP_011520058.1:n.*405_*406insGTC
XM_011521757.1:c.*405_*406insGTC (FANCI) XP_011520059.1:n.*405_*406insGTC
XM_011521758.1:c.*405_*406insGTC (FANCI) XP_011520060.1:n.*405_*406insGTC
XM_011521759.1:c.*405_*406insGTC (FANCI) XP_011520061.1:n.*405_*406insGTC
XM_011521760.1:c.*405_*406insGTC (FANCI) XP_011520062.1:n.*405_*406insGTC
XM_011521761.1:c.*405_*406insGTC (FANCI) XP_011520063.1:n.*405_*406insGTC
XM_011521762.1:c.*405_*406insGTC (FANCI) XP_011520064.1:n.*405_*406insGTC
XM_011521763.1:c.*405_*406insGTC (FANCI) XP_011520065.1:n.*405_*406insGTC
XM_011521764.1:c.*405_*406insGTC (FANCI) XP_011520066.1:n.*405_*406insGTC
XM_011521765.1:c.*405_*406insGTC (FANCI) XP_011520067.1:n.*405_*406insGTC
XM_011521766.1:c.*405_*406insGTC (FANCI) XP_011520068.1:n.*405_*406insGTC
XM_011521767.1:c.*405_*406insGTC (FANCI) XP_011520069.1:n.*405_*406insGTC
XM_011521769.1:c.*405_*406insGTC (FANCI) XP_011520071.1:n.*405_*406insGTC
XM_011521756.2:c.*405_*406insGTC (FANCI) XP_011520058.1:n.*405_*406insGTC
XM_011521757.2:c.*405_*406insGTC (FANCI) XP_011520059.1:n.*405_*406insGTC
XM_011521764.2:c.*405_*406insGTC (FANCI) XP_011520066.1:n.*405_*406insGTC
XM_011521767.2:c.*405_*406insGTC (FANCI) XP_011520069.1:n.*405_*406insGTC
NM_001113378.2:c.*405_*406insGTC (FANCI) MANE Select NP_001106849.1:n.*405_*406insGTC
NM_001126131.2:c.3644-38_3644-37insGAC (POLG) NP_001119603.1:n.3644-38_3644-37insGAC
NM_001376910.1:c.*405_*406insGTC (FANCI) NP_001363839.1:n.*405_*406insGTC
NM_001376911.1:c.*405_*406insGTC (FANCI) NP_001363840.1:n.*405_*406insGTC
NM_018193.3:c.*405_*406insGTC (FANCI) NP_060663.2:n.*405_*406insGTC
NM_002693.3:c.3644-38_3644-37insGAC (POLG) MANE Select NP_002684.1:n.3644-38_3644-37insGAC