Canonical Allele Identifier: CA2123849173

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240452T= , CM000676.2:g.24240452T=	GRCh38
NC_000014.8:g.24709658T= , CM000676.1:g.24709658T=	GRCh37
NC_000014.7:g.23779498T=	NCBI36
NG_016650.1:g.7223A=
NG_054634.1:g.13036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1331A=
ENST00000557921.3:c.920A=	ENSP00000453157.3:p.Asn307=
ENST00000699682.1:n.1418A=
ENST00000699683.1:n.1468A=
ENST00000699684.1:c.*621A=	ENSP00000514523.1:n.*621A=
ENST00000699685.1:n.1232A=
ENST00000699686.1:c.821A=	ENSP00000514524.1:p.Asn274=
ENST00000699687.1:c.923A=	ENSP00000514525.1:p.Asn308=
ENST00000699688.1:n.1228A=
ENST00000699689.1:n.1584A=
ENST00000699690.1:n.1781A=
ENST00000699691.1:n.1925A=
ENST00000699693.1:n.1445A=
ENST00000699694.1:n.1687A=
ENST00000699695.1:c.*400A=	ENSP00000514526.1:n.*400A=
ENST00000699696.1:n.1331A=
ENST00000699697.1:c.1028A=	ENSP00000514527.1:p.Asn343=
ENST00000699698.1:n.949A=
ENST00000699699.1:n.1352A=
ENST00000699700.1:n.1475A=
ENST00000699701.1:c.*408A=	ENSP00000514528.1:n.*408A=
ENST00000267415.12:c.1028A= MANE Select	ENSP00000267415.7:p.Asn343=
ENST00000646753.1:c.923A=	ENSP00000494065.1:p.Asn308=
ENST00000267415.11:c.1028A=	ENSP00000267415.7:p.Asn343=
ENST00000399423.8:c.1028A=	ENSP00000382350.4:p.Asn343=
ENST00000557915.1:n.147A=
ENST00000558566.1:c.*400A=	ENSP00000453025.1:n.*400A=
ENST00000559969.5:c.786A=
ENST00000560019.5:c.23A=	ENSP00000453113.1:p.Asn8=
ENST00000626689.2:c.*400A=	ENSP00000486681.1:n.*400A=
NM_001099274.1:c.1028A=	NP_001092744.1:p.Asn343=
NM_012461.2:c.1028A=	NP_036593.2:p.Asn343=
XM_005267528.2:c.1028A=	XP_005267585.1:p.Asn343=
XM_005267529.2:c.923A=	XP_005267586.1:p.Asn308=
NM_001099274.2:c.1028A=	NP_001092744.1:p.Asn343=
NM_001363668.1:c.923A=	NP_001350597.1:p.Asn308=
NM_012461.3:c.1028A=	NP_036593.2:p.Asn343=
XM_011536642.2:c.*408A=	XP_011534944.1:n.*408A=
XM_017021216.2:c.386A=	XP_016876705.1:p.Asn129=
XM_017021217.1:c.386A=	XP_016876706.1:p.Asn129=
NM_001099274.3:c.1028A= MANE Select	NP_001092744.1:p.Asn343=
NM_001363668.2:c.923A=	NP_001350597.1:p.Asn308=