Canonical Allele Identifier: CA2281035521

Gene: TGIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.3457442G= , CM000680.2:g.3457442G=	GRCh38
NC_000018.9:g.3457440G= , CM000680.1:g.3457440G=	GRCh37
NC_000018.8:g.3447440G=	NCBI36
NG_007447.1:g.50369G=
NG_007447.2:g.50369G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330513.10:c.261G=	ENSP00000327959.6:p.Gln87=
ENST00000343820.10:c.321G= MANE Select	ENSP00000339631.6:p.Gln107=
ENST00000330513.9:c.708G=	ENSP00000327959.5:p.Gln236=
ENST00000343820.9:c.321G=	ENSP00000339631.5:p.Gln107=
ENST00000345133.9:c.261G=	ENSP00000343969.5:p.Gln87=
ENST00000400167.6:c.261G=	ENSP00000383031.2:p.Gln87=
ENST00000401449.5:c.261G=	ENSP00000385206.1:p.Gln87=
ENST00000405385.7:c.261G=	ENSP00000384970.2:p.Gln87=
ENST00000407501.6:c.321G=	ENSP00000384133.2:p.Gln107=
ENST00000472042.1:c.261G=	ENSP00000449501.1:p.Gln87=
ENST00000546979.5:c.321G=	ENSP00000448934.1:p.Gln107=
ENST00000548489.6:c.261G=	ENSP00000447747.2:p.Gln87=
ENST00000549253.5:c.261G=	ENSP00000449973.1:p.Gln87=
ENST00000549468.5:c.261G=	ENSP00000449722.1:p.Gln87=
ENST00000549546.5:c.261G=	ENSP00000449580.1:p.Gln87=
ENST00000549780.5:c.261G=	ENSP00000448121.1:p.Gln87=
ENST00000550958.5:c.261G=	ENSP00000449531.1:p.Gln87=
ENST00000551333.1:c.261G=	ENSP00000446838.1:p.Gln87=
ENST00000551541.5:c.261G=	ENSP00000450025.1:p.Gln87=
ENST00000552383.5:c.261G=	ENSP00000449287.1:p.Gln87=
ENST00000577543.5:c.*34G=	ENSP00000462285.1:n.*34G=
ENST00000618001.4:c.363G=	ENSP00000483499.1:p.Gln121=
NM_001278682.1:c.330G=	NP_001265611.1:p.Gln110=
NM_001278684.1:c.321G=	NP_001265613.1:p.Gln107=
NM_001278686.1:c.261G=	NP_001265615.1:p.Gln87=
NM_003244.3:c.321G=	NP_003235.1:p.Gln107=
NM_170695.3:c.708G=	NP_733796.2:p.Gln236=
NM_173207.2:c.363G=	NP_775299.1:p.Gln121=
NM_173208.2:c.321G=	NP_775300.1:p.Gln107=
NM_173209.2:c.261G=	NP_775301.1:p.Gln87=
NM_173210.2:c.261G=	NP_775302.1:p.Gln87=
NM_173211.1:c.261G=	NP_775303.1:p.Gln87=
NM_174886.2:c.261G=	NP_777480.1:p.Gln87=
XM_011525735.1:c.261G=	XP_011524037.1:p.Gln87=
XM_011525735.2:c.261G=	XP_011524037.1:p.Gln87=
XM_017025958.1:c.321G=	XP_016881447.1:p.Gln107=
XM_017025959.1:c.261G=	XP_016881448.1:p.Gln87=
NM_001278682.2:c.330G=	NP_001265611.1:p.Gln110=
NM_001278684.2:c.321G=	NP_001265613.1:p.Gln107=
NM_001278686.2:c.261G=	NP_001265615.1:p.Gln87=
NM_001374396.1:c.261G=	NP_001361325.1:p.Gln87=
NM_001374397.1:c.261G=	NP_001361326.1:p.Gln87=
NM_003244.4:c.321G= MANE Select	NP_003235.1:p.Gln107=
NM_170695.5:c.261G=	NP_733796.3:p.Gln87=
NM_173207.4:c.363G=	NP_775299.1:p.Gln121=
NM_173208.3:c.321G=	NP_775300.1:p.Gln107=
NM_173209.3:c.261G=	NP_775301.1:p.Gln87=
NM_173210.4:c.261G=	NP_775302.1:p.Gln87=
NM_173211.2:c.261G=	NP_775303.1:p.Gln87=
NM_174886.3:c.261G=	NP_777480.1:p.Gln87=
NM_001278686.3:c.261G=	NP_001265615.1:p.Gln87=