Canonical Allele Identifier: CA391222097

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104712834A>G , CM000676.2:g.104712834A>G	GRCh38
NC_000014.8:g.105179171A>G , CM000676.1:g.105179171A>G	GRCh37
NC_000014.7:g.104250216A>G	NCBI36
NG_027684.1:g.28229A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.2617A>G MANE Select	NP_071934.3:p.Ile873Val
ENST00000392634.9:c.2617A>G MANE Select	ENSP00000376410.4:p.Ile873Val
NM_001031714.3:c.2617A>G	NP_001026884.3:p.Ile873Val
NM_001031714.4:c.2617A>G	NP_001026884.3:p.Ile873Val
NM_022489.3:c.2617A>G	NP_071934.3:p.Ile873Val
ENST00000252527.8:c.1021A>G	ENSP00000252527.8:p.Ile341Val
ENST00000330634.11:c.2617A>G	ENSP00000376406.3:p.Ile873Val
ENST00000392634.8:c.2617A>G	ENSP00000376410.4:p.Ile873Val
ENST00000477497.1:n.122A>G
ENST00000480763.2:n.482A>G
ENST00000617571.4:c.-1517A>G	ENSP00000483829.1:n.-1517A>G
ENST00000617571.5:c.2617A>G	ENSP00000483829.2:p.Ile873Val
ENST00000674520.1:c.2612A>G	ENSP00000502593.1:p.His871Arg
ENST00000674631.1:c.655A>G	ENSP00000502830.1:p.Ile219Val
ENST00000674662.1:c.2621A>G	ENSP00000501895.1:n.2621A>G
ENST00000674757.1:c.2617A>G	ENSP00000502202.1:p.Ile873Val
ENST00000674822.1:c.2501A>G	ENSP00000501552.1:n.2501A>G
ENST00000674846.1:c.2612A>G	ENSP00000502431.1:n.2612A>G
ENST00000674857.1:c.2606A>G	ENSP00000501687.1:n.2606A>G
ENST00000674960.1:c.2475A>G	ENSP00000501841.1:n.2475A>G
ENST00000674991.1:c.1867A>G	ENSP00000502004.1:p.Ile623Val
ENST00000674994.1:c.2583A>G	ENSP00000502442.1:n.2583A>G
ENST00000675207.1:c.2713A>G	ENSP00000502644.1:p.Ile905Val
ENST00000675329.1:c.2593A>G	ENSP00000502287.1:p.Ile865Val
ENST00000675481.1:c.2617A>G	ENSP00000502723.1:p.Ile873Val
ENST00000675557.1:n.396A>G
ENST00000675583.1:c.2546A>G	ENSP00000501740.1:n.2546A>G
ENST00000675638.1:c.2617A>G	ENSP00000501647.1:p.Ile873Val
ENST00000675724.1:c.2555A>G	ENSP00000502576.1:n.2555A>G
ENST00000675771.1:c.1880A>G	ENSP00000502104.1:n.1880A>G
ENST00000675797.1:c.2022A>G	ENSP00000502023.1:n.2022A>G
ENST00000675809.1:c.2672A>G	ENSP00000502587.1:n.2672A>G
ENST00000675930.1:c.2617A>G	ENSP00000502456.1:p.Ile873Val
ENST00000675980.1:c.2635A>G	ENSP00000502520.1:p.Ile879Val
ENST00000676016.1:c.2516A>G	ENSP00000502412.1:n.2516A>G
ENST00000676366.1:c.2617A>G	ENSP00000501605.1:p.Ile873Val
XM_005268004.3:c.2713A>G	XP_005268061.1:p.Ile905Val
XM_005268004.4:c.2713A>G	XP_005268061.1:p.Ile905Val
XM_005268005.3:c.2713A>G	XP_005268062.1:p.Ile905Val
XM_005268005.4:c.2713A>G	XP_005268062.1:p.Ile905Val
XM_017021595.1:c.2713A>G	XP_016877084.1:p.Ile905Val
XR_943507.1:n.2842A>G