Canonical Allele Identifier: CA2575682143

Gene: INF2

Linked Data

• gnomAD v4: 14-104703230-AGGGCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104703241_104703246del , CM000676.2:g.104703241_104703246del	GRCh38
NC_000014.8:g.105169578_105169583del , CM000676.1:g.105169578_105169583del	GRCh37
NC_000014.7:g.104240623_104240628del	NCBI36
NG_027684.1:g.18636_18641del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392634.9:c.507+21_507+26del MANE Select	ENSP00000376410.4:n.507+21_507+26del
ENST00000617571.5:c.507+21_507+26del	ENSP00000483829.2:n.507+21_507+26del
ENST00000674520.1:c.507+21_507+26del	ENSP00000502593.1:n.507+21_507+26del
ENST00000674662.1:c.507+21_507+26del	ENSP00000501895.1:n.507+21_507+26del
ENST00000674757.1:c.507+21_507+26del	ENSP00000502202.1:n.507+21_507+26del
ENST00000674822.1:c.392-54_392-49del	ENSP00000501552.1:n.392-54_392-49del
ENST00000674846.1:c.507+21_507+26del	ENSP00000502431.1:n.507+21_507+26del
ENST00000674857.1:c.507+21_507+26del	ENSP00000501687.1:n.507+21_507+26del
ENST00000674960.1:c.507+21_507+26del	ENSP00000501841.1:n.507+21_507+26del
ENST00000674991.1:c.507+21_507+26del	ENSP00000502004.1:n.507+21_507+26del
ENST00000674994.1:c.507+21_507+26del	ENSP00000502442.1:n.507+21_507+26del
ENST00000675029.1:n.709+21_709+26del
ENST00000675207.1:c.603+21_603+26del	ENSP00000502644.1:n.603+21_603+26del
ENST00000675329.1:c.507+21_507+26del	ENSP00000502287.1:n.507+21_507+26del
ENST00000675481.1:c.507+21_507+26del	ENSP00000502723.1:n.507+21_507+26del
ENST00000675583.1:c.507+21_507+26del	ENSP00000501740.1:n.507+21_507+26del
ENST00000675638.1:c.507+21_507+26del	ENSP00000501647.1:n.507+21_507+26del
ENST00000675724.1:c.507+21_507+26del	ENSP00000502576.1:n.507+21_507+26del
ENST00000675771.1:c.507+21_507+26del	ENSP00000502104.1:n.507+21_507+26del
ENST00000675797.1:c.507+21_507+26del	ENSP00000502023.1:n.507+21_507+26del
ENST00000675809.1:c.507+21_507+26del	ENSP00000502587.1:n.507+21_507+26del
ENST00000675930.1:c.507+21_507+26del	ENSP00000502456.1:n.507+21_507+26del
ENST00000675980.1:c.507+21_507+26del	ENSP00000502520.1:n.507+21_507+26del
ENST00000676016.1:c.507+21_507+26del	ENSP00000502412.1:n.507+21_507+26del
ENST00000676366.1:c.507+21_507+26del	ENSP00000501605.1:n.507+21_507+26del
ENST00000330634.11:c.507+21_507+26del	ENSP00000376406.3:n.507+21_507+26del
ENST00000392634.8:c.507+21_507+26del	ENSP00000376410.4:n.507+21_507+26del
ENST00000398337.8:c.507+21_507+26del	ENSP00000381380.4:n.507+21_507+26del
NM_001031714.3:c.507+21_507+26del	NP_001026884.3:n.507+21_507+26del
NM_022489.3:c.507+21_507+26del	NP_071934.3:n.507+21_507+26del
NM_032714.2:c.507+21_507+26del	NP_116103.1:n.507+21_507+26del
XM_005268004.3:c.603+21_603+26del	XP_005268061.1:n.603+21_603+26del
XM_005268005.3:c.603+21_603+26del	XP_005268062.1:n.603+21_603+26del
XR_943507.1:n.732+21_732+26del
XM_005268004.4:c.603+21_603+26del	XP_005268061.1:n.603+21_603+26del
XM_005268005.4:c.603+21_603+26del	XP_005268062.1:n.603+21_603+26del
XM_017021595.1:c.603+21_603+26del	XP_016877084.1:n.603+21_603+26del
XR_001750518.1:n.708+21_708+26del
NM_001031714.4:c.507+21_507+26del	NP_001026884.3:n.507+21_507+26del
NM_022489.4:c.507+21_507+26del MANE Select	NP_071934.3:n.507+21_507+26del
NM_032714.3:c.507+21_507+26del	NP_116103.1:n.507+21_507+26del