Canonical Allele Identifier: CA8875993
Gene: TGIF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399122
ClinVar RCV Id: RCV001893721
dbSNP Id: rs759756166
gnomAD v2: 18-3457728-A-G
gnomAD v3: 18-3457730-A-G
gnomAD v4: 18-3457730-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.3457730A>G , CM000680.2:g.3457730A>G GRCh38
NC_000018.9:g.3457728A>G , CM000680.1:g.3457728A>G GRCh37
NC_000018.8:g.3447728A>G NCBI36
NG_007447.1:g.50657A>G
NG_007447.2:g.50657A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330513.10:c.549A>G ENSP00000327959.6:p.Ile183Met
ENST00000343820.10:c.609A>G MANE Select ENSP00000339631.6:p.Ile203Met
ENST00000330513.9:c.996A>G ENSP00000327959.5:p.Ile332Met
ENST00000343820.9:c.609A>G ENSP00000339631.5:p.Ile203Met
ENST00000345133.9:c.549A>G ENSP00000343969.5:p.Ile183Met
ENST00000400167.6:c.549A>G ENSP00000383031.2:p.Ile183Met
ENST00000401449.5:c.549A>G ENSP00000385206.1:p.Ile183Met
ENST00000405385.7:c.549A>G ENSP00000384970.2:p.Ile183Met
ENST00000407501.6:c.609A>G ENSP00000384133.2:p.Ile203Met
ENST00000472042.1:c.549A>G ENSP00000449501.1:p.Ile183Met
ENST00000548489.6:c.549A>G ENSP00000447747.2:p.Ile183Met
ENST00000549546.5:c.549A>G ENSP00000449580.1:p.Ile183Met
ENST00000549780.5:c.549A>G ENSP00000448121.1:p.Ile183Met
ENST00000551541.5:c.549A>G ENSP00000450025.1:p.Ile183Met
ENST00000618001.4:c.651A>G ENSP00000483499.1:p.Ile217Met
NM_001278682.1:c.618A>G NP_001265611.1:p.Ile206Met
NM_001278684.1:c.609A>G NP_001265613.1:p.Ile203Met
NM_001278686.1:c.549A>G NP_001265615.1:p.Ile183Met
NM_003244.3:c.609A>G NP_003235.1:p.Ile203Met
NM_170695.3:c.996A>G NP_733796.2:p.Ile332Met
NM_173207.2:c.651A>G NP_775299.1:p.Ile217Met
NM_173208.2:c.609A>G NP_775300.1:p.Ile203Met
NM_173209.2:c.549A>G NP_775301.1:p.Ile183Met
NM_173210.2:c.549A>G NP_775302.1:p.Ile183Met
NM_173211.1:c.549A>G NP_775303.1:p.Ile183Met
NM_174886.2:c.549A>G NP_777480.1:p.Ile183Met
XM_011525735.1:c.549A>G XP_011524037.1:p.Ile183Met
XM_011525735.2:c.549A>G XP_011524037.1:p.Ile183Met
XM_017025958.1:c.609A>G XP_016881447.1:p.Ile203Met
XM_017025959.1:c.549A>G XP_016881448.1:p.Ile183Met
NM_001278682.2:c.618A>G NP_001265611.1:p.Ile206Met
NM_001278684.2:c.609A>G NP_001265613.1:p.Ile203Met
NM_001278686.2:c.549A>G NP_001265615.1:p.Ile183Met
NM_001374396.1:c.549A>G NP_001361325.1:p.Ile183Met
NM_001374397.1:c.549A>G NP_001361326.1:p.Ile183Met
NM_003244.4:c.609A>G MANE Select NP_003235.1:p.Ile203Met
NM_170695.5:c.549A>G NP_733796.3:p.Ile183Met
NM_173207.4:c.651A>G NP_775299.1:p.Ile217Met
NM_173208.3:c.609A>G NP_775300.1:p.Ile203Met
NM_173209.3:c.549A>G NP_775301.1:p.Ile183Met
NM_173210.4:c.549A>G NP_775302.1:p.Ile183Met
NM_173211.2:c.549A>G NP_775303.1:p.Ile183Met
NM_174886.3:c.549A>G NP_777480.1:p.Ile183Met
NM_001278686.3:c.549A>G NP_001265615.1:p.Ile183Met