Canonical Allele Identifier: CA391222742

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104713265C>T , CM000676.2:g.104713265C>T	GRCh38
NC_000014.8:g.105179602C>T , CM000676.1:g.105179602C>T	GRCh37
NC_000014.7:g.104250647C>T	NCBI36
NG_027684.1:g.28660C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.2834C>T MANE Select	NP_071934.3:p.Ala945Val
ENST00000392634.9:c.2834C>T MANE Select	ENSP00000376410.4:p.Ala945Val
NM_001031714.3:c.2834C>T	NP_001026884.3:p.Ala945Val
NM_001031714.4:c.2834C>T	NP_001026884.3:p.Ala945Val
NM_022489.3:c.2834C>T	NP_071934.3:p.Ala945Val
ENST00000252527.8:c.1238C>T	ENSP00000252527.8:p.Ala413Val
ENST00000330634.11:c.2834C>T	ENSP00000376406.3:p.Ala945Val
ENST00000392634.8:c.2834C>T	ENSP00000376410.4:p.Ala945Val
ENST00000477497.1:n.339C>T
ENST00000617571.4:c.-1300C>T	ENSP00000483829.1:n.-1300C>T
ENST00000617571.5:c.2834C>T	ENSP00000483829.2:p.Ala945Val
ENST00000674520.1:c.2829C>T	ENSP00000502593.1:n.2829C>T
ENST00000674631.1:c.872C>T	ENSP00000502830.1:p.Ala291Val
ENST00000674662.1:c.2838C>T	ENSP00000501895.1:n.2838C>T
ENST00000674757.1:c.2839C>T	ENSP00000502202.1:p.Arg947Trp
ENST00000674822.1:c.2718C>T	ENSP00000501552.1:n.2718C>T
ENST00000674846.1:c.2829C>T	ENSP00000502431.1:n.2829C>T
ENST00000674857.1:c.2823C>T	ENSP00000501687.1:n.2823C>T
ENST00000674960.1:c.2692C>T	ENSP00000501841.1:n.2692C>T
ENST00000674991.1:c.2084C>T	ENSP00000502004.1:p.Ala695Val
ENST00000674994.1:c.2800C>T	ENSP00000502442.1:n.2800C>T
ENST00000675207.1:c.2930C>T	ENSP00000502644.1:p.Ala977Val
ENST00000675329.1:c.2810C>T	ENSP00000502287.1:p.Ala937Val
ENST00000675481.1:c.2834C>T	ENSP00000502723.1:p.Ala945Val
ENST00000675583.1:c.2763C>T	ENSP00000501740.1:n.2763C>T
ENST00000675638.1:c.2834C>T	ENSP00000501647.1:p.Ala945Val
ENST00000675724.1:c.2772C>T	ENSP00000502576.1:n.2772C>T
ENST00000675771.1:c.2097C>T	ENSP00000502104.1:n.2097C>T
ENST00000675797.1:c.2239C>T	ENSP00000502023.1:n.2239C>T
ENST00000675809.1:c.2889C>T	ENSP00000502587.1:n.2889C>T
ENST00000675930.1:c.2834C>T	ENSP00000502456.1:p.Ala945Val
ENST00000675980.1:c.2852C>T	ENSP00000502520.1:p.Ala951Val
ENST00000676016.1:c.2733C>T	ENSP00000502412.1:n.2733C>T
ENST00000676366.1:c.2834C>T	ENSP00000501605.1:p.Ala945Val
XM_005268004.3:c.2930C>T	XP_005268061.1:p.Ala977Val
XM_005268004.4:c.2930C>T	XP_005268061.1:p.Ala977Val
XM_005268005.3:c.2930C>T	XP_005268062.1:p.Ala977Val
XM_005268005.4:c.2930C>T	XP_005268062.1:p.Ala977Val
XM_017021595.1:c.2930C>T	XP_016877084.1:p.Ala977Val
XR_943507.1:n.3059C>T