Canonical Allele Identifier: CA401723455

Gene: TGIF1

Linked Data

• COSMIC: COSM6259798 ; COSM6259799
• MyVariant Identifiers: chr18:g.3457522G>T (hg19) ; chr18:g.3457524G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.3457524G>T , CM000680.2:g.3457524G>T	GRCh38
NC_000018.9:g.3457522G>T , CM000680.1:g.3457522G>T	GRCh37
NC_000018.8:g.3447522G>T	NCBI36
NG_007447.1:g.50451G>T
NG_007447.2:g.50451G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330513.10:c.343G>T	ENSP00000327959.6:p.Ala115Ser
ENST00000343820.10:c.403G>T MANE Select	ENSP00000339631.6:p.Ala135Ser
ENST00000330513.9:c.790G>T	ENSP00000327959.5:p.Ala264Ser
ENST00000343820.9:c.403G>T	ENSP00000339631.5:p.Ala135Ser
ENST00000345133.9:c.343G>T	ENSP00000343969.5:p.Ala115Ser
ENST00000400167.6:c.343G>T	ENSP00000383031.2:p.Ala115Ser
ENST00000401449.5:c.343G>T	ENSP00000385206.1:p.Ala115Ser
ENST00000405385.7:c.343G>T	ENSP00000384970.2:p.Ala115Ser
ENST00000407501.6:c.403G>T	ENSP00000384133.2:p.Ala135Ser
ENST00000472042.1:c.343G>T	ENSP00000449501.1:p.Ala115Ser
ENST00000548489.6:c.343G>T	ENSP00000447747.2:p.Ala115Ser
ENST00000549468.5:c.343G>T	ENSP00000449722.1:p.Ala115Ser
ENST00000549546.5:c.343G>T	ENSP00000449580.1:p.Ala115Ser
ENST00000549780.5:c.343G>T	ENSP00000448121.1:p.Ala115Ser
ENST00000550958.5:c.343G>T	ENSP00000449531.1:p.Ala115Ser
ENST00000551333.1:c.343G>T	ENSP00000446838.1:p.Ala115Ser
ENST00000551541.5:c.343G>T	ENSP00000450025.1:p.Ala115Ser
ENST00000552383.5:c.343G>T	ENSP00000449287.1:p.Ala115Ser
ENST00000577543.5:c.*116G>T	ENSP00000462285.1:n.*116G>T
ENST00000618001.4:c.445G>T	ENSP00000483499.1:p.Ala149Ser
NM_001278682.1:c.412G>T	NP_001265611.1:p.Ala138Ser
NM_001278684.1:c.403G>T	NP_001265613.1:p.Ala135Ser
NM_001278686.1:c.343G>T	NP_001265615.1:p.Ala115Ser
NM_003244.3:c.403G>T	NP_003235.1:p.Ala135Ser
NM_170695.3:c.790G>T	NP_733796.2:p.Ala264Ser
NM_173207.2:c.445G>T	NP_775299.1:p.Ala149Ser
NM_173208.2:c.403G>T	NP_775300.1:p.Ala135Ser
NM_173209.2:c.343G>T	NP_775301.1:p.Ala115Ser
NM_173210.2:c.343G>T	NP_775302.1:p.Ala115Ser
NM_173211.1:c.343G>T	NP_775303.1:p.Ala115Ser
NM_174886.2:c.343G>T	NP_777480.1:p.Ala115Ser
XM_011525735.1:c.343G>T	XP_011524037.1:p.Ala115Ser
XM_011525735.2:c.343G>T	XP_011524037.1:p.Ala115Ser
XM_017025958.1:c.403G>T	XP_016881447.1:p.Ala135Ser
XM_017025959.1:c.343G>T	XP_016881448.1:p.Ala115Ser
NM_001278682.2:c.412G>T	NP_001265611.1:p.Ala138Ser
NM_001278684.2:c.403G>T	NP_001265613.1:p.Ala135Ser
NM_001278686.2:c.343G>T	NP_001265615.1:p.Ala115Ser
NM_001374396.1:c.343G>T	NP_001361325.1:p.Ala115Ser
NM_001374397.1:c.343G>T	NP_001361326.1:p.Ala115Ser
NM_003244.4:c.403G>T MANE Select	NP_003235.1:p.Ala135Ser
NM_170695.5:c.343G>T	NP_733796.3:p.Ala115Ser
NM_173207.4:c.445G>T	NP_775299.1:p.Ala149Ser
NM_173208.3:c.403G>T	NP_775300.1:p.Ala135Ser
NM_173209.3:c.343G>T	NP_775301.1:p.Ala115Ser
NM_173210.4:c.343G>T	NP_775302.1:p.Ala115Ser
NM_173211.2:c.343G>T	NP_775303.1:p.Ala115Ser
NM_174886.3:c.343G>T	NP_777480.1:p.Ala115Ser
NM_001278686.3:c.343G>T	NP_001265615.1:p.Ala115Ser