Canonical Allele Identifier: CA2626814976

Gene: INF2

Linked Data

• gnomAD v4: 14-104701330-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104701330T>C , CM000676.2:g.104701330T>C	GRCh38
NC_000014.8:g.105167667T>C , CM000676.1:g.105167667T>C	GRCh37
NC_000014.7:g.104238712T>C	NCBI36
NG_027684.1:g.16725T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392634.9:c.-9-27T>C MANE Select	ENSP00000376410.4:n.-9-27T>C
ENST00000674723.1:c.-9-27T>C	ENSP00000502257.1:n.-9-27T>C
ENST00000674869.1:c.-9-27T>C	ENSP00000501558.1:n.-9-27T>C
ENST00000674966.1:n.460-27T>C
ENST00000675207.1:c.88-27T>C	ENSP00000502644.1:n.88-27T>C
ENST00000675313.1:n.33-27T>C
ENST00000675482.1:c.-9-27T>C	ENSP00000501798.1:n.-9-27T>C
ENST00000675616.1:n.32-27T>C
ENST00000676100.1:n.129-27T>C
ENST00000676427.1:c.-9-27T>C	ENSP00000502106.1:n.-9-27T>C
ENST00000330634.11:c.-9-27T>C	ENSP00000376406.3:n.-9-27T>C
ENST00000392634.8:c.-9-27T>C	ENSP00000376410.4:n.-9-27T>C
ENST00000398337.8:c.-9-27T>C	ENSP00000381380.4:n.-9-27T>C
NM_001031714.3:c.-9-27T>C	NP_001026884.3:n.-9-27T>C
NM_022489.3:c.-9-27T>C	NP_071934.3:n.-9-27T>C
NM_032714.2:c.-9-27T>C	NP_116103.1:n.-9-27T>C
XM_005268004.3:c.88-27T>C	XP_005268061.1:n.88-27T>C
XM_005268005.3:c.88-27T>C	XP_005268062.1:n.88-27T>C
XR_943507.1:n.217-27T>C
XM_005268004.4:c.88-27T>C	XP_005268061.1:n.88-27T>C
XM_005268005.4:c.88-27T>C	XP_005268062.1:n.88-27T>C
XM_017021595.1:c.88-27T>C	XP_016877084.1:n.88-27T>C
XR_001750518.1:n.193-27T>C
NM_001031714.4:c.-9-27T>C	NP_001026884.3:n.-9-27T>C
NM_022489.4:c.-9-27T>C MANE Select	NP_071934.3:n.-9-27T>C
NM_032714.3:c.-9-27T>C	NP_116103.1:n.-9-27T>C