Canonical Allele Identifier: CA7373066

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104713005G>A , CM000676.2:g.104713005G>A	GRCh38
NC_000014.8:g.105179342G>A , CM000676.1:g.105179342G>A	GRCh37
NC_000014.7:g.104250387G>A	NCBI36
NG_027684.1:g.28400G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.2775+13G>A MANE Select	NP_071934.3:n.2775+13G>A
ENST00000392634.9:c.2775+13G>A MANE Select	ENSP00000376410.4:n.2775+13G>A
NM_001031714.3:c.2775+13G>A	NP_001026884.3:n.2775+13G>A
NM_001031714.4:c.2775+13G>A	NP_001026884.3:n.2775+13G>A
NM_022489.3:c.2775+13G>A	NP_071934.3:n.2775+13G>A
ENST00000252527.8:c.1179+13G>A	ENSP00000252527.8:n.1179+13G>A
ENST00000330634.11:c.2775+13G>A	ENSP00000376406.3:n.2775+13G>A
ENST00000392634.8:c.2775+13G>A	ENSP00000376410.4:n.2775+13G>A
ENST00000477497.1:n.280+13G>A
ENST00000617571.4:c.-1359+13G>A	ENSP00000483829.1:n.-1359+13G>A
ENST00000617571.5:c.2775+13G>A	ENSP00000483829.2:n.2775+13G>A
ENST00000674520.1:c.2770+13G>A	ENSP00000502593.1:n.2770+13G>A
ENST00000674631.1:c.813+13G>A	ENSP00000502830.1:n.813+13G>A
ENST00000674662.1:c.2779+13G>A	ENSP00000501895.1:n.2779+13G>A
ENST00000674757.1:c.2775+13G>A	ENSP00000502202.1:n.2775+13G>A
ENST00000674822.1:c.2659+13G>A	ENSP00000501552.1:n.2659+13G>A
ENST00000674846.1:c.2770+13G>A	ENSP00000502431.1:n.2770+13G>A
ENST00000674857.1:c.2764+13G>A	ENSP00000501687.1:n.2764+13G>A
ENST00000674960.1:c.2633+13G>A	ENSP00000501841.1:n.2633+13G>A
ENST00000674991.1:c.2025+13G>A	ENSP00000502004.1:n.2025+13G>A
ENST00000674994.1:c.2741+13G>A	ENSP00000502442.1:n.2741+13G>A
ENST00000675207.1:c.2871+13G>A	ENSP00000502644.1:n.2871+13G>A
ENST00000675329.1:c.2751+13G>A	ENSP00000502287.1:n.2751+13G>A
ENST00000675481.1:c.2775+13G>A	ENSP00000502723.1:n.2775+13G>A
ENST00000675583.1:c.2704+13G>A	ENSP00000501740.1:n.2704+13G>A
ENST00000675638.1:c.2775+13G>A	ENSP00000501647.1:n.2775+13G>A
ENST00000675724.1:c.2713+13G>A	ENSP00000502576.1:n.2713+13G>A
ENST00000675771.1:c.2038+13G>A	ENSP00000502104.1:n.2038+13G>A
ENST00000675797.1:c.2180+13G>A	ENSP00000502023.1:n.2180+13G>A
ENST00000675809.1:c.2830+13G>A	ENSP00000502587.1:n.2830+13G>A
ENST00000675930.1:c.2775+13G>A	ENSP00000502456.1:n.2775+13G>A
ENST00000675980.1:c.2793+13G>A	ENSP00000502520.1:n.2793+13G>A
ENST00000676016.1:c.2674+13G>A	ENSP00000502412.1:n.2674+13G>A
ENST00000676366.1:c.2775+13G>A	ENSP00000501605.1:n.2775+13G>A
XM_005268004.3:c.2871+13G>A	XP_005268061.1:n.2871+13G>A
XM_005268004.4:c.2871+13G>A	XP_005268061.1:n.2871+13G>A
XM_005268005.3:c.2871+13G>A	XP_005268062.1:n.2871+13G>A
XM_005268005.4:c.2871+13G>A	XP_005268062.1:n.2871+13G>A
XM_017021595.1:c.2871+13G>A	XP_016877084.1:n.2871+13G>A
XR_943507.1:n.3000+13G>A