Canonical Allele Identifier: CA7373274

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104714640G>A , CM000676.2:g.104714640G>A	GRCh38
NC_000014.8:g.105180977G>A , CM000676.1:g.105180977G>A	GRCh37
NC_000014.7:g.104252022G>A	NCBI36
NG_027684.1:g.30035G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392634.9:c.3478G>A MANE Select	ENSP00000376410.4:p.Gly1160Ser
ENST00000617571.5:c.3474G>A	ENSP00000483829.2:n.3474G>A
ENST00000674520.1:c.3473G>A	ENSP00000502593.1:n.3473G>A
ENST00000674631.1:c.1516G>A	ENSP00000502830.1:p.Gly506Ser
ENST00000674662.1:c.3482G>A	ENSP00000501895.1:n.3482G>A
ENST00000674757.1:c.3483G>A	ENSP00000502202.1:n.3483G>A
ENST00000674822.1:c.3362G>A	ENSP00000501552.1:n.3362G>A
ENST00000674846.1:c.3473G>A	ENSP00000502431.1:n.3473G>A
ENST00000674857.1:c.3467G>A	ENSP00000501687.1:n.3467G>A
ENST00000674960.1:c.3336G>A	ENSP00000501841.1:n.3336G>A
ENST00000674991.1:c.2728G>A	ENSP00000502004.1:p.Gly910Ser
ENST00000675207.1:c.3574G>A	ENSP00000502644.1:p.Gly1192Ser
ENST00000675329.1:c.3454G>A	ENSP00000502287.1:p.Gly1152Ser
ENST00000675481.1:c.3478G>A	ENSP00000502723.1:p.Gly1160Ser
ENST00000675583.1:c.3407G>A	ENSP00000501740.1:n.3407G>A
ENST00000675603.1:n.718G>A
ENST00000675638.1:c.3397G>A	ENSP00000501647.1:p.Gly1133Ser
ENST00000675724.1:c.3416G>A	ENSP00000502576.1:n.3416G>A
ENST00000675771.1:c.2741G>A	ENSP00000502104.1:n.2741G>A
ENST00000675797.1:c.2883G>A	ENSP00000502023.1:n.2883G>A
ENST00000675809.1:c.3533G>A	ENSP00000502587.1:n.3533G>A
ENST00000675930.1:c.3366G>A	ENSP00000502456.1:p.Val1122=
ENST00000675980.1:c.3496G>A	ENSP00000502520.1:p.Gly1166Ser
ENST00000676016.1:c.3377G>A	ENSP00000502412.1:n.3377G>A
ENST00000676366.1:c.3285G>A	ENSP00000501605.1:p.Val1095=
ENST00000252527.8:c.1882G>A	ENSP00000252527.8:p.Gly628Ser
ENST00000330634.11:c.3478G>A	ENSP00000376406.3:p.Gly1160Ser
ENST00000392634.8:c.3478G>A	ENSP00000376410.4:p.Gly1160Ser
ENST00000617571.4:c.-656G>A	ENSP00000483829.1:n.-656G>A
NM_001031714.3:c.3478G>A	NP_001026884.3:p.Gly1160Ser
NM_022489.3:c.3478G>A	NP_071934.3:p.Gly1160Ser
XM_005268004.3:c.3574G>A	XP_005268061.1:p.Gly1192Ser
XM_005268005.3:c.3574G>A	XP_005268062.1:p.Gly1192Ser
XR_943507.1:n.3703G>A
XM_005268004.4:c.3574G>A	XP_005268061.1:p.Gly1192Ser
XM_005268005.4:c.3574G>A	XP_005268062.1:p.Gly1192Ser
XM_017021595.1:c.3574G>A	XP_016877084.1:p.Gly1192Ser
NM_001031714.4:c.3478G>A	NP_001026884.3:p.Gly1160Ser
NM_022489.4:c.3478G>A MANE Select	NP_071934.3:p.Gly1160Ser