Canonical Allele Identifier: CA7373443

Gene: INF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104718809C>T , CM000676.2:g.104718809C>T	GRCh38
NC_000014.8:g.105185146C>T , CM000676.1:g.105185146C>T	GRCh37
NC_000014.7:g.104256191C>T	NCBI36
NG_027684.1:g.34204C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392634.9:c.*16C>T MANE Select	ENSP00000376410.4:n.*16C>T
ENST00000617571.5:c.3762C>T	ENSP00000483829.2:n.3762C>T
ENST00000674686.1:c.171C>T
ENST00000675207.1:c.*16C>T	ENSP00000502644.1:n.*16C>T
ENST00000675424.1:c.257C>T
ENST00000675638.1:c.3685C>T	ENSP00000501647.1:n.3685C>T
ENST00000252527.8:c.2254C>T	ENSP00000252527.8:n.2254C>T
ENST00000330634.11:c.3709C>T	ENSP00000376406.3:p.Pro1237Ser
ENST00000392634.8:c.*16C>T	ENSP00000376410.4:n.*16C>T
ENST00000481338.1:n.308C>T
ENST00000617571.4:c.-368C>T	ENSP00000483829.1:n.-368C>T
NM_001031714.3:c.3709C>T	NP_001026884.3:p.Pro1237Ser
NM_022489.3:c.*16C>T	NP_071934.3:n.*16C>T
XM_005268004.3:c.*16C>T	XP_005268061.1:n.*16C>T
XM_005268005.3:c.3805C>T	XP_005268062.1:p.Pro1269Ser
XR_943507.1:n.4075C>T
XM_005268004.4:c.*16C>T	XP_005268061.1:n.*16C>T
XM_005268005.4:c.3805C>T	XP_005268062.1:p.Pro1269Ser
NM_001031714.4:c.3709C>T	NP_001026884.3:p.Pro1237Ser
NM_022489.4:c.*16C>T MANE Select	NP_071934.3:n.*16C>T