Canonical Allele Identifier: CA2123849132

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240435_24240436delinsCA , CM000676.2:g.24240435_24240436delinsCA	GRCh38
NC_000014.8:g.24709641_24709642delinsCA , CM000676.1:g.24709641_24709642delinsCA	GRCh37
NC_000014.7:g.23779481_23779482delinsCA	NCBI36
NG_016650.1:g.7239_7240delinsTG
NG_054634.1:g.13019_13020delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1347_1348delinsTG
ENST00000557921.3:c.936_937delinsTG	ENSP00000453157.3:p.Pro312=
ENST00000699682.1:n.1434_1435delinsTG
ENST00000699683.1:n.1484_1485delinsTG
ENST00000699684.1:c.*637_*638delinsTG	ENSP00000514523.1:n.*637_*638delinsTG
ENST00000699685.1:n.1248_1249delinsTG
ENST00000699686.1:c.837_838delinsTG	ENSP00000514524.1:p.Pro279=
ENST00000699687.1:c.939_940delinsTG	ENSP00000514525.1:p.Pro313=
ENST00000699688.1:n.1244_1245delinsTG
ENST00000699689.1:n.1600_1601delinsTG
ENST00000699690.1:n.1797_1798delinsTG
ENST00000699691.1:n.1941_1942delinsTG
ENST00000699693.1:n.1461_1462delinsTG
ENST00000699694.1:n.1703_1704delinsTG
ENST00000699695.1:c.*416_*417delinsTG	ENSP00000514526.1:n.*416_*417delinsTG
ENST00000699696.1:n.1347_1348delinsTG
ENST00000699697.1:c.1044_1045delinsTG	ENSP00000514527.1:p.Pro348=
ENST00000699698.1:n.965_966delinsTG
ENST00000699699.1:n.1368_1369delinsTG
ENST00000699700.1:n.1491_1492delinsTG
ENST00000699701.1:c.*424_*425delinsTG	ENSP00000514528.1:n.*424_*425delinsTG
ENST00000267415.12:c.1044_1045delinsTG MANE Select	ENSP00000267415.7:p.Pro348=
ENST00000646753.1:c.939_940delinsTG	ENSP00000494065.1:p.Pro313=
ENST00000267415.11:c.1044_1045delinsTG	ENSP00000267415.7:p.Pro348=
ENST00000399423.8:c.1044_1045delinsTG	ENSP00000382350.4:p.Pro348=
ENST00000557915.1:n.163_164delinsTG
ENST00000558566.1:c.*416_*417delinsTG	ENSP00000453025.1:n.*416_*417delinsTG
ENST00000559969.5:c.802_803delinsTG
ENST00000560019.5:c.39_40delinsTG	ENSP00000453113.1:p.Pro13=
ENST00000626689.2:c.*416_*417delinsTG	ENSP00000486681.1:n.*416_*417delinsTG
NM_001099274.1:c.1044_1045delinsTG	NP_001092744.1:p.Pro348=
NM_012461.2:c.1044_1045delinsTG	NP_036593.2:p.Pro348=
XM_005267528.2:c.1044_1045delinsTG	XP_005267585.1:p.Pro348=
XM_005267529.2:c.939_940delinsTG	XP_005267586.1:p.Pro313=
NM_001099274.2:c.1044_1045delinsTG	NP_001092744.1:p.Pro348=
NM_001363668.1:c.939_940delinsTG	NP_001350597.1:p.Pro313=
NM_012461.3:c.1044_1045delinsTG	NP_036593.2:p.Pro348=
XM_011536642.2:c.*424_*425delinsTG	XP_011534944.1:n.*424_*425delinsTG
XM_017021216.2:c.402_403delinsTG	XP_016876705.1:p.Pro134=
XM_017021217.1:c.402_403delinsTG	XP_016876706.1:p.Pro134=
NM_001099274.3:c.1044_1045delinsTG MANE Select	NP_001092744.1:p.Pro348=
NM_001363668.2:c.939_940delinsTG	NP_001350597.1:p.Pro313=