Canonical Allele Identifier: CA7373092

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104713235C>T , CM000676.2:g.104713235C>T	GRCh38
NC_000014.8:g.105179572C>T , CM000676.1:g.105179572C>T	GRCh37
NC_000014.7:g.104250617C>T	NCBI36
NG_027684.1:g.28630C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022489.4:c.2804C>T MANE Select	NP_071934.3:p.Ala935Val
ENST00000392634.9:c.2804C>T MANE Select	ENSP00000376410.4:p.Ala935Val
NM_001031714.3:c.2804C>T	NP_001026884.3:p.Ala935Val
NM_001031714.4:c.2804C>T	NP_001026884.3:p.Ala935Val
NM_022489.3:c.2804C>T	NP_071934.3:p.Ala935Val
ENST00000252527.8:c.1208C>T	ENSP00000252527.8:p.Ala403Val
ENST00000330634.11:c.2804C>T	ENSP00000376406.3:p.Ala935Val
ENST00000392634.8:c.2804C>T	ENSP00000376410.4:p.Ala935Val
ENST00000477497.1:n.309C>T
ENST00000617571.4:c.-1330C>T	ENSP00000483829.1:n.-1330C>T
ENST00000617571.5:c.2804C>T	ENSP00000483829.2:p.Ala935Val
ENST00000674520.1:c.2799C>T	ENSP00000502593.1:n.2799C>T
ENST00000674631.1:c.842C>T	ENSP00000502830.1:p.Ala281Val
ENST00000674662.1:c.2808C>T	ENSP00000501895.1:n.2808C>T
ENST00000674757.1:c.2809C>T	ENSP00000502202.1:p.Arg937Ter
ENST00000674822.1:c.2688C>T	ENSP00000501552.1:n.2688C>T
ENST00000674846.1:c.2799C>T	ENSP00000502431.1:n.2799C>T
ENST00000674857.1:c.2793C>T	ENSP00000501687.1:n.2793C>T
ENST00000674960.1:c.2662C>T	ENSP00000501841.1:n.2662C>T
ENST00000674991.1:c.2054C>T	ENSP00000502004.1:p.Ala685Val
ENST00000674994.1:c.2770C>T	ENSP00000502442.1:n.2770C>T
ENST00000675207.1:c.2900C>T	ENSP00000502644.1:p.Ala967Val
ENST00000675329.1:c.2780C>T	ENSP00000502287.1:p.Ala927Val
ENST00000675481.1:c.2804C>T	ENSP00000502723.1:p.Ala935Val
ENST00000675583.1:c.2733C>T	ENSP00000501740.1:n.2733C>T
ENST00000675638.1:c.2804C>T	ENSP00000501647.1:p.Ala935Val
ENST00000675724.1:c.2742C>T	ENSP00000502576.1:n.2742C>T
ENST00000675771.1:c.2067C>T	ENSP00000502104.1:n.2067C>T
ENST00000675797.1:c.2209C>T	ENSP00000502023.1:n.2209C>T
ENST00000675809.1:c.2859C>T	ENSP00000502587.1:n.2859C>T
ENST00000675930.1:c.2804C>T	ENSP00000502456.1:p.Ala935Val
ENST00000675980.1:c.2822C>T	ENSP00000502520.1:p.Ala941Val
ENST00000676016.1:c.2703C>T	ENSP00000502412.1:n.2703C>T
ENST00000676366.1:c.2804C>T	ENSP00000501605.1:p.Ala935Val
XM_005268004.3:c.2900C>T	XP_005268061.1:p.Ala967Val
XM_005268004.4:c.2900C>T	XP_005268061.1:p.Ala967Val
XM_005268005.3:c.2900C>T	XP_005268062.1:p.Ala967Val
XM_005268005.4:c.2900C>T	XP_005268062.1:p.Ala967Val
XM_017021595.1:c.2900C>T	XP_016877084.1:p.Ala967Val
XR_943507.1:n.3029C>T