Canonical Allele Identifier: CA7373336

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104714816C>T , CM000676.2:g.104714816C>T	GRCh38
NC_000014.8:g.105181153C>T , CM000676.1:g.105181153C>T	GRCh37
NC_000014.7:g.104252198C>T	NCBI36
NG_027684.1:g.30211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392634.9:c.3654C>T MANE Select	ENSP00000376410.4:p.Thr1218=
ENST00000617571.5:c.3650C>T	ENSP00000483829.2:n.3650C>T
ENST00000674520.1:c.3649C>T	ENSP00000502593.1:n.3649C>T
ENST00000674631.1:c.1692C>T	ENSP00000502830.1:p.Thr564=
ENST00000674662.1:c.3658C>T	ENSP00000501895.1:n.3658C>T
ENST00000674757.1:c.3659C>T	ENSP00000502202.1:n.3659C>T
ENST00000674822.1:c.3538C>T	ENSP00000501552.1:n.3538C>T
ENST00000674846.1:c.3649C>T	ENSP00000502431.1:n.3649C>T
ENST00000674857.1:c.3643C>T	ENSP00000501687.1:n.3643C>T
ENST00000674960.1:c.3512C>T	ENSP00000501841.1:n.3512C>T
ENST00000674991.1:c.2904C>T	ENSP00000502004.1:p.Thr968=
ENST00000675207.1:c.3750C>T	ENSP00000502644.1:p.Thr1250=
ENST00000675329.1:c.3630C>T	ENSP00000502287.1:p.Thr1210=
ENST00000675481.1:c.3654C>T	ENSP00000502723.1:p.Thr1218=
ENST00000675583.1:c.3583C>T	ENSP00000501740.1:n.3583C>T
ENST00000675603.1:n.894C>T
ENST00000675638.1:c.3573C>T	ENSP00000501647.1:p.Thr1191=
ENST00000675724.1:c.3592C>T	ENSP00000502576.1:n.3592C>T
ENST00000675771.1:c.2917C>T	ENSP00000502104.1:n.2917C>T
ENST00000675797.1:c.3059C>T	ENSP00000502023.1:n.3059C>T
ENST00000675809.1:c.3709C>T	ENSP00000502587.1:n.3709C>T
ENST00000675930.1:c.3542C>T	ENSP00000502456.1:n.3542C>T
ENST00000675980.1:c.3672C>T	ENSP00000502520.1:p.Thr1224=
ENST00000676016.1:c.3553C>T	ENSP00000502412.1:n.3553C>T
ENST00000676366.1:c.3461C>T	ENSP00000501605.1:n.3461C>T
ENST00000252527.8:c.2058C>T	ENSP00000252527.8:p.Thr686=
ENST00000330634.11:c.3654C>T	ENSP00000376406.3:p.Thr1218=
ENST00000392634.8:c.3654C>T	ENSP00000376410.4:p.Thr1218=
ENST00000617571.4:c.-480C>T	ENSP00000483829.1:n.-480C>T
NM_001031714.3:c.3654C>T	NP_001026884.3:p.Thr1218=
NM_022489.3:c.3654C>T	NP_071934.3:p.Thr1218=
XM_005268004.3:c.3750C>T	XP_005268061.1:p.Thr1250=
XM_005268005.3:c.3750C>T	XP_005268062.1:p.Thr1250=
XR_943507.1:n.3879C>T
XM_005268004.4:c.3750C>T	XP_005268061.1:p.Thr1250=
XM_005268005.4:c.3750C>T	XP_005268062.1:p.Thr1250=
XM_017021595.1:c.3750C>T	XP_016877084.1:p.Thr1250=
NM_001031714.4:c.3654C>T	NP_001026884.3:p.Thr1218=
NM_022489.4:c.3654C>T MANE Select	NP_071934.3:p.Thr1218=