Canonical Allele Identifier: CA7373261

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104714623A>T , CM000676.2:g.104714623A>T	GRCh38
NC_000014.8:g.105180960A>T , CM000676.1:g.105180960A>T	GRCh37
NC_000014.7:g.104252005A>T	NCBI36
NG_027684.1:g.30018A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.3461A>T MANE Select	NP_071934.3:p.Asp1154Val
ENST00000392634.9:c.3461A>T MANE Select	ENSP00000376410.4:p.Asp1154Val
NM_001031714.3:c.3461A>T	NP_001026884.3:p.Asp1154Val
NM_001031714.4:c.3461A>T	NP_001026884.3:p.Asp1154Val
NM_022489.3:c.3461A>T	NP_071934.3:p.Asp1154Val
ENST00000252527.8:c.1865A>T	ENSP00000252527.8:p.Asp622Val
ENST00000330634.11:c.3461A>T	ENSP00000376406.3:p.Asp1154Val
ENST00000392634.8:c.3461A>T	ENSP00000376410.4:p.Asp1154Val
ENST00000617571.4:c.-673A>T	ENSP00000483829.1:n.-673A>T
ENST00000617571.5:c.3457A>T	ENSP00000483829.2:n.3457A>T
ENST00000674520.1:c.3456A>T	ENSP00000502593.1:n.3456A>T
ENST00000674631.1:c.1499A>T	ENSP00000502830.1:p.Asp500Val
ENST00000674662.1:c.3465A>T	ENSP00000501895.1:n.3465A>T
ENST00000674757.1:c.3466A>T	ENSP00000502202.1:n.3466A>T
ENST00000674822.1:c.3345A>T	ENSP00000501552.1:n.3345A>T
ENST00000674846.1:c.3456A>T	ENSP00000502431.1:n.3456A>T
ENST00000674857.1:c.3450A>T	ENSP00000501687.1:n.3450A>T
ENST00000674960.1:c.3319A>T	ENSP00000501841.1:n.3319A>T
ENST00000674991.1:c.2711A>T	ENSP00000502004.1:p.Asp904Val
ENST00000675207.1:c.3557A>T	ENSP00000502644.1:p.Asp1186Val
ENST00000675329.1:c.3437A>T	ENSP00000502287.1:p.Asp1146Val
ENST00000675481.1:c.3461A>T	ENSP00000502723.1:p.Asp1154Val
ENST00000675583.1:c.3390A>T	ENSP00000501740.1:n.3390A>T
ENST00000675603.1:n.701A>T
ENST00000675638.1:c.3380A>T	ENSP00000501647.1:p.Asp1127Val
ENST00000675724.1:c.3399A>T	ENSP00000502576.1:n.3399A>T
ENST00000675771.1:c.2724A>T	ENSP00000502104.1:n.2724A>T
ENST00000675797.1:c.2866A>T	ENSP00000502023.1:n.2866A>T
ENST00000675809.1:c.3516A>T	ENSP00000502587.1:n.3516A>T
ENST00000675930.1:c.3349A>T	ENSP00000502456.1:p.Thr1117Ser
ENST00000675980.1:c.3479A>T	ENSP00000502520.1:p.Asp1160Val
ENST00000676016.1:c.3360A>T	ENSP00000502412.1:n.3360A>T
ENST00000676366.1:c.3268A>T	ENSP00000501605.1:p.Thr1090Ser
XM_005268004.3:c.3557A>T	XP_005268061.1:p.Asp1186Val
XM_005268004.4:c.3557A>T	XP_005268061.1:p.Asp1186Val
XM_005268005.3:c.3557A>T	XP_005268062.1:p.Asp1186Val
XM_005268005.4:c.3557A>T	XP_005268062.1:p.Asp1186Val
XM_017021595.1:c.3557A>T	XP_016877084.1:p.Asp1186Val
XR_943507.1:n.3686A>T