Canonical Allele Identifier: CA254028
Gene: TGIF1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6981
ClinVar RCV Id: RCV000007396
dbSNP Id: rs121909068

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.3457572A>G , CM000680.2:g.3457572A>G GRCh38
NC_000018.9:g.3457570A>G , CM000680.1:g.3457570A>G GRCh37
NC_000018.8:g.3447570A>G NCBI36
NG_007447.1:g.50499A>G

Transcript Alleles

HGVS Amino-acid change
NM_001278682.1:c.460A>G VV NP_001265611.1:p.Thr154Ala
NM_001278684.1:c.451A>G VV NP_001265613.1:p.Thr151Ala
NM_001278686.1:c.391A>G VV NP_001265615.1:p.Thr131Ala
NM_003244.3:c.451A>G VV NP_003235.1:p.Thr151Ala
NM_170695.3:c.838A>G VV NP_733796.2:p.Thr280Ala
NM_173207.2:c.493A>G VV NP_775299.1:p.Thr165Ala
NM_173208.2:c.451A>G VV NP_775300.1:p.Thr151Ala
NM_173209.2:c.391A>G VV NP_775301.1:p.Thr131Ala
NM_173210.2:c.391A>G VV NP_775302.1:p.Thr131Ala
NM_173211.1:c.391A>G VV NP_775303.1:p.Thr131Ala
NM_174886.2:c.391A>G VV NP_777480.1:p.Thr131Ala
XM_011525735.1:c.391A>G XP_011524037.1:p.Thr131Ala
XM_011525735.2:c.391A>G
XM_017025958.1:c.451A>G XP_016881447.1:p.Thr151Ala
XM_017025959.1:c.391A>G XP_016881448.1:p.Thr131Ala
ENST00000330513.9:c.838A>G ENSP00000327959.5:p.Thr280Ala
ENST00000343820.9:c.451A>G ENSP00000339631.5:p.Thr151Ala
ENST00000345133.9:c.391A>G ENSP00000343969.5:p.Thr131Ala
ENST00000400167.6:c.391A>G ENSP00000383031.2:p.Thr131Ala
ENST00000401449.5:c.391A>G ENSP00000385206.1:p.Thr131Ala
ENST00000405385.7:c.391A>G ENSP00000384970.2:p.Thr131Ala
ENST00000407501.6:c.451A>G ENSP00000384133.2:p.Thr151Ala
ENST00000472042.1:c.391A>G ENSP00000449501.1:p.Thr131Ala
ENST00000548489.6:c.391A>G ENSP00000447747.2:p.Thr131Ala
ENST00000549468.5:c.391A>G ENSP00000449722.1:p.Thr131Ala
ENST00000549546.5:c.391A>G ENSP00000449580.1:p.Thr131Ala
ENST00000549780.5:c.391A>G ENSP00000448121.1:p.Thr131Ala
ENST00000550958.5:c.391A>G ENSP00000449531.1:p.Thr131Ala
ENST00000551333.1:c.391A>G ENSP00000446838.1:p.Thr131Ala
ENST00000551541.5:c.391A>G ENSP00000450025.1:p.Thr131Ala
ENST00000552383.5:c.391A>G ENSP00000449287.1:p.Thr131Ala
ENST00000577543.5:c.*164A>G ENSP00000462285.1:p.=
ENST00000618001.4:c.493A>G ENSP00000483499.1:p.Thr165Ala