Canonical Allele Identifier: CA7372983

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104712515G>A , CM000676.2:g.104712515G>A	GRCh38
NC_000014.8:g.105178852G>A , CM000676.1:g.105178852G>A	GRCh37
NC_000014.7:g.104249897G>A	NCBI36
NG_027684.1:g.27910G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.2572G>A MANE Select	NP_071934.3:p.Val858Met
ENST00000392634.9:c.2572G>A MANE Select	ENSP00000376410.4:p.Val858Met
NM_001031714.3:c.2572G>A	NP_001026884.3:p.Val858Met
NM_001031714.4:c.2572G>A	NP_001026884.3:p.Val858Met
NM_022489.3:c.2572G>A	NP_071934.3:p.Val858Met
ENST00000252527.8:c.976G>A	ENSP00000252527.8:p.Val326Met
ENST00000330634.11:c.2572G>A	ENSP00000376406.3:p.Val858Met
ENST00000392634.8:c.2572G>A	ENSP00000376410.4:p.Val858Met
ENST00000480763.2:n.437G>A
ENST00000617571.4:c.-1562G>A	ENSP00000483829.1:n.-1562G>A
ENST00000617571.5:c.2572G>A	ENSP00000483829.2:p.Val858Met
ENST00000674520.1:c.2572G>A	ENSP00000502593.1:p.Val858Met
ENST00000674631.1:c.610G>A	ENSP00000502830.1:p.Val204Met
ENST00000674662.1:c.2576G>A	ENSP00000501895.1:n.2576G>A
ENST00000674757.1:c.2572G>A	ENSP00000502202.1:p.Val858Met
ENST00000674822.1:c.2456G>A	ENSP00000501552.1:n.2456G>A
ENST00000674846.1:c.2567G>A	ENSP00000502431.1:n.2567G>A
ENST00000674857.1:c.2561G>A	ENSP00000501687.1:n.2561G>A
ENST00000674960.1:c.2430G>A	ENSP00000501841.1:n.2430G>A
ENST00000674991.1:c.1822G>A	ENSP00000502004.1:p.Val608Met
ENST00000674994.1:c.2538G>A	ENSP00000502442.1:n.2538G>A
ENST00000675207.1:c.2668G>A	ENSP00000502644.1:p.Val890Met
ENST00000675329.1:c.2548G>A	ENSP00000502287.1:p.Val850Met
ENST00000675481.1:c.2572G>A	ENSP00000502723.1:p.Val858Met
ENST00000675557.1:n.351G>A
ENST00000675583.1:c.2501G>A	ENSP00000501740.1:n.2501G>A
ENST00000675638.1:c.2572G>A	ENSP00000501647.1:p.Val858Met
ENST00000675724.1:c.2510G>A	ENSP00000502576.1:n.2510G>A
ENST00000675771.1:c.1835G>A	ENSP00000502104.1:n.1835G>A
ENST00000675797.1:c.1977G>A	ENSP00000502023.1:n.1977G>A
ENST00000675809.1:c.2627G>A	ENSP00000502587.1:n.2627G>A
ENST00000675930.1:c.2572G>A	ENSP00000502456.1:p.Val858Met
ENST00000675980.1:c.2590G>A	ENSP00000502520.1:p.Val864Met
ENST00000676016.1:c.2471G>A	ENSP00000502412.1:n.2471G>A
ENST00000676366.1:c.2572G>A	ENSP00000501605.1:p.Val858Met
XM_005268004.3:c.2668G>A	XP_005268061.1:p.Val890Met
XM_005268004.4:c.2668G>A	XP_005268061.1:p.Val890Met
XM_005268005.3:c.2668G>A	XP_005268062.1:p.Val890Met
XM_005268005.4:c.2668G>A	XP_005268062.1:p.Val890Met
XM_017021595.1:c.2668G>A	XP_016877084.1:p.Val890Met
XR_943507.1:n.2797G>A