Canonical Allele Identifier: CA2123849054

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240374G= , CM000676.2:g.24240374G=	GRCh38
NC_000014.8:g.24709580G= , CM000676.1:g.24709580G=	GRCh37
NC_000014.7:g.23779420G=	NCBI36
NG_016650.1:g.7301C=
NG_054634.1:g.12958G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1409C=
ENST00000557921.3:c.*41C=	ENSP00000453157.3:n.*41C=
ENST00000699682.1:n.1496C=
ENST00000699683.1:n.1546C=
ENST00000699684.1:c.*699C=	ENSP00000514523.1:n.*699C=
ENST00000699685.1:n.1310C=
ENST00000699686.1:c.*41C=	ENSP00000514524.1:n.*41C=
ENST00000699687.1:c.*41C=	ENSP00000514525.1:n.*41C=
ENST00000699688.1:n.1306C=
ENST00000699689.1:n.1662C=
ENST00000699690.1:n.1859C=
ENST00000699691.1:n.2003C=
ENST00000699693.1:n.1479-44C=
ENST00000699694.1:n.1765C=
ENST00000699695.1:c.*434-44C=	ENSP00000514526.1:n.*434-44C=
ENST00000699696.1:n.1409C=
ENST00000699697.1:c.1062-44C=	ENSP00000514527.1:n.1062-44C=
ENST00000699698.1:n.983-44C=
ENST00000699699.1:n.1430C=
ENST00000699700.1:n.1553C=
ENST00000699701.1:c.*486C=	ENSP00000514528.1:n.*486C=
ENST00000267415.12:c.1062-44C= MANE Select	ENSP00000267415.7:n.1062-44C=
ENST00000646753.1:c.957-44C=	ENSP00000494065.1:n.957-44C=
ENST00000267415.11:c.1062-44C=	ENSP00000267415.7:n.1062-44C=
ENST00000399423.8:c.*41C=	ENSP00000382350.4:n.*41C=
ENST00000557915.1:n.225C=
ENST00000558566.1:c.*478C=	ENSP00000453025.1:n.*478C=
ENST00000559969.5:c.864C=
ENST00000560019.5:c.57-44C=	ENSP00000453113.1:n.57-44C=
ENST00000626689.2:c.*434-44C=	ENSP00000486681.1:n.*434-44C=
NM_001099274.1:c.1062-44C=	NP_001092744.1:n.1062-44C=
NM_012461.2:c.*41C=	NP_036593.2:n.*41C=
XM_005267528.2:c.1062-44C=	XP_005267585.1:n.1062-44C=
XM_005267529.2:c.957-44C=	XP_005267586.1:n.957-44C=
NM_001099274.2:c.1062-44C=	NP_001092744.1:n.1062-44C=
NM_001363668.1:c.957-44C=	NP_001350597.1:n.957-44C=
NM_012461.3:c.*41C=	NP_036593.2:n.*41C=
XM_011536642.2:c.*486C=	XP_011534944.1:n.*486C=
XM_017021216.2:c.420-44C=	XP_016876705.1:n.420-44C=
XM_017021217.1:c.420-44C=	XP_016876706.1:n.420-44C=
NM_001099274.3:c.1062-44C= MANE Select	NP_001092744.1:n.1062-44C=
NM_001363668.2:c.957-44C=	NP_001350597.1:n.957-44C=