Canonical Allele Identifier: CA7373191

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104714315C>T , CM000676.2:g.104714315C>T	GRCh38
NC_000014.8:g.105180652C>T , CM000676.1:g.105180652C>T	GRCh37
NC_000014.7:g.104251697C>T	NCBI36
NG_027684.1:g.29710C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392634.9:c.3153C>T MANE Select	ENSP00000376410.4:p.Asp1051=
ENST00000617571.5:c.3149C>T	ENSP00000483829.2:n.3149C>T
ENST00000674520.1:c.3148C>T	ENSP00000502593.1:n.3148C>T
ENST00000674631.1:c.1191C>T	ENSP00000502830.1:p.Asp397=
ENST00000674662.1:c.3157C>T	ENSP00000501895.1:n.3157C>T
ENST00000674757.1:c.3158C>T	ENSP00000502202.1:n.3158C>T
ENST00000674822.1:c.3037C>T	ENSP00000501552.1:n.3037C>T
ENST00000674846.1:c.3148C>T	ENSP00000502431.1:n.3148C>T
ENST00000674857.1:c.3142C>T	ENSP00000501687.1:n.3142C>T
ENST00000674960.1:c.3011C>T	ENSP00000501841.1:n.3011C>T
ENST00000674991.1:c.2403C>T	ENSP00000502004.1:p.Asp801=
ENST00000675207.1:c.3249C>T	ENSP00000502644.1:p.Asp1083=
ENST00000675329.1:c.3129C>T	ENSP00000502287.1:p.Asp1043=
ENST00000675481.1:c.3153C>T	ENSP00000502723.1:p.Asp1051=
ENST00000675583.1:c.3082C>T	ENSP00000501740.1:n.3082C>T
ENST00000675603.1:n.393C>T
ENST00000675638.1:c.3072C>T	ENSP00000501647.1:p.Asp1024=
ENST00000675724.1:c.3091C>T	ENSP00000502576.1:n.3091C>T
ENST00000675771.1:c.2416C>T	ENSP00000502104.1:n.2416C>T
ENST00000675797.1:c.2558C>T	ENSP00000502023.1:n.2558C>T
ENST00000675809.1:c.3208C>T	ENSP00000502587.1:n.3208C>T
ENST00000675930.1:c.3153C>T	ENSP00000502456.1:p.Asp1051=
ENST00000675980.1:c.3171C>T	ENSP00000502520.1:p.Asp1057=
ENST00000676016.1:c.3052C>T	ENSP00000502412.1:n.3052C>T
ENST00000676366.1:c.3153C>T	ENSP00000501605.1:p.Asp1051=
ENST00000252527.8:c.1557C>T	ENSP00000252527.8:p.Asp519=
ENST00000330634.11:c.3153C>T	ENSP00000376406.3:p.Asp1051=
ENST00000392634.8:c.3153C>T	ENSP00000376410.4:p.Asp1051=
ENST00000617571.4:c.-981C>T	ENSP00000483829.1:n.-981C>T
NM_001031714.3:c.3153C>T	NP_001026884.3:p.Asp1051=
NM_022489.3:c.3153C>T	NP_071934.3:p.Asp1051=
XM_005268004.3:c.3249C>T	XP_005268061.1:p.Asp1083=
XM_005268005.3:c.3249C>T	XP_005268062.1:p.Asp1083=
XR_943507.1:n.3378C>T
XM_005268004.4:c.3249C>T	XP_005268061.1:p.Asp1083=
XM_005268005.4:c.3249C>T	XP_005268062.1:p.Asp1083=
XM_017021595.1:c.3249C>T	XP_016877084.1:p.Asp1083=
NM_001031714.4:c.3153C>T	NP_001026884.3:p.Asp1051=
NM_022489.4:c.3153C>T MANE Select	NP_071934.3:p.Asp1051=