Canonical Allele Identifier: CA2838267891

Gene: IFFO1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6541451T>G , CM000674.2:g.6541451T>G	GRCh38
NC_000012.11:g.6650617T>G , CM000674.1:g.6650617T>G	GRCh37
NC_000012.10:g.6520878T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619571.5:c.1610+61A>C MANE Select	ENSP00000482285.1:n.1610+61A>C
ENST00000336604.8:c.1583+61A>C	ENSP00000337593.4:n.1583+61A>C
ENST00000356896.8:c.1586+61A>C	ENSP00000349364.4:n.1586+61A>C
ENST00000396830.2:n.794+61A>C
ENST00000396840.6:c.1574+61A>C	ENSP00000380052.2:n.1574+61A>C
ENST00000436152.6:c.665+61A>C	ENSP00000390721.2:n.665+61A>C
ENST00000465801.5:c.662+61A>C	ENSP00000436261.1:n.662+61A>C
ENST00000471408.5:n.1215+61A>C
ENST00000472558.6:n.943+61A>C
ENST00000487279.6:c.*888+61A>C	ENSP00000432493.2:n.*888+61A>C
ENST00000488007.5:n.1989+61A>C
ENST00000615885.4:c.665+61A>C	ENSP00000482340.1:n.665+61A>C
ENST00000619571.4:c.1610+61A>C	ENSP00000482285.1:n.1610+61A>C
NM_001039670.2:c.1586+61A>C	NP_001034759.1:n.1586+61A>C
NM_001193457.1:c.1610+61A>C	NP_001180386.1:n.1610+61A>C
NM_080730.4:c.1583+61A>C	NP_542768.2:n.1583+61A>C
NR_036467.1:n.1737+61A>C
XM_006718973.2:c.1607+61A>C	XP_006719036.1:n.1607+61A>C
XM_006718975.2:c.1583+61A>C	XP_006719038.1:n.1583+61A>C
XM_006718976.2:c.1577+61A>C	XP_006719039.1:n.1577+61A>C
XM_006718977.2:c.1574+61A>C	XP_006719040.1:n.1574+61A>C
XM_006718981.2:c.662+61A>C	XP_006719044.1:n.662+61A>C
XM_011520945.1:c.1874+61A>C	XP_011519247.1:n.1874+61A>C
XM_011520946.1:c.1871+61A>C	XP_011519248.1:n.1871+61A>C
XM_011520947.1:c.1850+61A>C	XP_011519249.1:n.1850+61A>C
XM_011520948.1:c.1847+61A>C	XP_011519250.1:n.1847+61A>C
XM_011520949.1:c.1841+61A>C	XP_011519251.1:n.1841+61A>C
XM_011520951.1:c.953+61A>C	XP_011519253.1:n.953+61A>C
XM_011520952.1:c.926+61A>C	XP_011519254.1:n.926+61A>C
NM_001330324.1:c.1574+61A>C	NP_001317253.1:n.1574+61A>C
NM_001330325.1:c.1580+61A>C	NP_001317254.1:n.1580+61A>C
XM_006718975.4:c.1583+61A>C	XP_006719038.1:n.1583+61A>C
XM_006718976.4:c.1577+61A>C	XP_006719039.1:n.1577+61A>C
XM_006718981.3:c.662+61A>C	XP_006719044.1:n.662+61A>C
XM_011520947.3:c.1850+61A>C	XP_011519249.1:n.1850+61A>C
XM_011520948.3:c.1847+61A>C	XP_011519250.1:n.1847+61A>C
XM_011520949.3:c.1841+61A>C	XP_011519251.1:n.1841+61A>C
XM_011520952.2:c.926+61A>C	XP_011519254.1:n.926+61A>C
XM_017019170.1:c.1661+61A>C	XP_016874659.1:n.1661+61A>C
XM_017019172.1:c.929+61A>C	XP_016874661.1:n.929+61A>C
XM_017019173.1:c.920+61A>C	XP_016874662.1:n.920+61A>C
NM_001039670.3:c.1586+61A>C	NP_001034759.1:n.1586+61A>C
NM_001330324.2:c.1574+61A>C	NP_001317253.1:n.1574+61A>C
NM_001330325.2:c.1580+61A>C	NP_001317254.1:n.1580+61A>C
NM_080730.5:c.1583+61A>C	NP_542768.2:n.1583+61A>C
NR_036467.2:n.1696+61A>C
NM_001193457.2:c.1610+61A>C MANE Select	NP_001180386.1:n.1610+61A>C