Canonical Allele Identifier: CA7373042

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104712918G>A , CM000676.2:g.104712918G>A	GRCh38
NC_000014.8:g.105179255G>A , CM000676.1:g.105179255G>A	GRCh37
NC_000014.7:g.104250300G>A	NCBI36
NG_027684.1:g.28313G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.2701G>A MANE Select	NP_071934.3:p.Ala901Thr
ENST00000392634.9:c.2701G>A MANE Select	ENSP00000376410.4:p.Ala901Thr
NM_001031714.3:c.2701G>A	NP_001026884.3:p.Ala901Thr
NM_001031714.4:c.2701G>A	NP_001026884.3:p.Ala901Thr
NM_022489.3:c.2701G>A	NP_071934.3:p.Ala901Thr
ENST00000252527.8:c.1105G>A	ENSP00000252527.8:p.Ala369Thr
ENST00000330634.11:c.2701G>A	ENSP00000376406.3:p.Ala901Thr
ENST00000392634.8:c.2701G>A	ENSP00000376410.4:p.Ala901Thr
ENST00000477497.1:n.206G>A
ENST00000480763.2:n.566G>A
ENST00000617571.4:c.-1433G>A	ENSP00000483829.1:n.-1433G>A
ENST00000617571.5:c.2701G>A	ENSP00000483829.2:p.Ala901Thr
ENST00000674520.1:c.2696G>A	ENSP00000502593.1:n.2696G>A
ENST00000674631.1:c.739G>A	ENSP00000502830.1:p.Ala247Thr
ENST00000674662.1:c.2705G>A	ENSP00000501895.1:n.2705G>A
ENST00000674757.1:c.2701G>A	ENSP00000502202.1:p.Ala901Thr
ENST00000674822.1:c.2585G>A	ENSP00000501552.1:n.2585G>A
ENST00000674846.1:c.2696G>A	ENSP00000502431.1:n.2696G>A
ENST00000674857.1:c.2690G>A	ENSP00000501687.1:n.2690G>A
ENST00000674960.1:c.2559G>A	ENSP00000501841.1:n.2559G>A
ENST00000674991.1:c.1951G>A	ENSP00000502004.1:p.Ala651Thr
ENST00000674994.1:c.2667G>A	ENSP00000502442.1:n.2667G>A
ENST00000675207.1:c.2797G>A	ENSP00000502644.1:p.Ala933Thr
ENST00000675329.1:c.2677G>A	ENSP00000502287.1:p.Ala893Thr
ENST00000675481.1:c.2701G>A	ENSP00000502723.1:p.Ala901Thr
ENST00000675557.1:n.480G>A
ENST00000675583.1:c.2630G>A	ENSP00000501740.1:n.2630G>A
ENST00000675638.1:c.2701G>A	ENSP00000501647.1:p.Ala901Thr
ENST00000675724.1:c.2639G>A	ENSP00000502576.1:n.2639G>A
ENST00000675771.1:c.1964G>A	ENSP00000502104.1:n.1964G>A
ENST00000675797.1:c.2106G>A	ENSP00000502023.1:n.2106G>A
ENST00000675809.1:c.2756G>A	ENSP00000502587.1:n.2756G>A
ENST00000675930.1:c.2701G>A	ENSP00000502456.1:p.Ala901Thr
ENST00000675980.1:c.2719G>A	ENSP00000502520.1:p.Ala907Thr
ENST00000676016.1:c.2600G>A	ENSP00000502412.1:n.2600G>A
ENST00000676366.1:c.2701G>A	ENSP00000501605.1:p.Ala901Thr
XM_005268004.3:c.2797G>A	XP_005268061.1:p.Ala933Thr
XM_005268004.4:c.2797G>A	XP_005268061.1:p.Ala933Thr
XM_005268005.3:c.2797G>A	XP_005268062.1:p.Ala933Thr
XM_005268005.4:c.2797G>A	XP_005268062.1:p.Ala933Thr
XM_017021595.1:c.2797G>A	XP_016877084.1:p.Ala933Thr
XR_943507.1:n.2926G>A