Canonical Allele Identifier: CA2123849170
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240451G= , CM000676.2:g.24240451G= GRCh38
NC_000014.8:g.24709657G= , CM000676.1:g.24709657G= GRCh37
NC_000014.7:g.23779497G= NCBI36
NG_016650.1:g.7224C=
NG_054634.1:g.13035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1332C=
ENST00000557921.3:c.921C= ENSP00000453157.3:p.Asn307=
ENST00000699682.1:n.1419C=
ENST00000699683.1:n.1469C=
ENST00000699684.1:c.*622C= ENSP00000514523.1:n.*622C=
ENST00000699685.1:n.1233C=
ENST00000699686.1:c.822C= ENSP00000514524.1:p.Asn274=
ENST00000699687.1:c.924C= ENSP00000514525.1:p.Asn308=
ENST00000699688.1:n.1229C=
ENST00000699689.1:n.1585C=
ENST00000699690.1:n.1782C=
ENST00000699691.1:n.1926C=
ENST00000699693.1:n.1446C=
ENST00000699694.1:n.1688C=
ENST00000699695.1:c.*401C= ENSP00000514526.1:n.*401C=
ENST00000699696.1:n.1332C=
ENST00000699697.1:c.1029C= ENSP00000514527.1:p.Asn343=
ENST00000699698.1:n.950C=
ENST00000699699.1:n.1353C=
ENST00000699700.1:n.1476C=
ENST00000699701.1:c.*409C= ENSP00000514528.1:n.*409C=
ENST00000267415.12:c.1029C= MANE Select ENSP00000267415.7:p.Asn343=
ENST00000646753.1:c.924C= ENSP00000494065.1:p.Asn308=
ENST00000267415.11:c.1029C= ENSP00000267415.7:p.Asn343=
ENST00000399423.8:c.1029C= ENSP00000382350.4:p.Asn343=
ENST00000557915.1:n.148C=
ENST00000558566.1:c.*401C= ENSP00000453025.1:n.*401C=
ENST00000559969.5:c.787C=
ENST00000560019.5:c.24C= ENSP00000453113.1:p.Asn8=
ENST00000626689.2:c.*401C= ENSP00000486681.1:n.*401C=
NM_001099274.1:c.1029C= NP_001092744.1:p.Asn343=
NM_012461.2:c.1029C= NP_036593.2:p.Asn343=
XM_005267528.2:c.1029C= XP_005267585.1:p.Asn343=
XM_005267529.2:c.924C= XP_005267586.1:p.Asn308=
NM_001099274.2:c.1029C= NP_001092744.1:p.Asn343=
NM_001363668.1:c.924C= NP_001350597.1:p.Asn308=
NM_012461.3:c.1029C= NP_036593.2:p.Asn343=
XM_011536642.2:c.*409C= XP_011534944.1:n.*409C=
XM_017021216.2:c.387C= XP_016876705.1:p.Asn129=
XM_017021217.1:c.387C= XP_016876706.1:p.Asn129=
NM_001099274.3:c.1029C= MANE Select NP_001092744.1:p.Asn343=
NM_001363668.2:c.924C= NP_001350597.1:p.Asn308=