Canonical Allele Identifier: CA2123849099

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240409_24240411delinsTTC , CM000676.2:g.24240409_24240411delinsTTC	GRCh38
NC_000014.8:g.24709615_24709617delinsTTC , CM000676.1:g.24709615_24709617delinsTTC	GRCh37
NC_000014.7:g.23779455_23779457delinsTTC	NCBI36
NG_016650.1:g.7264_7266delinsGAA
NG_054634.1:g.12993_12995delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1372_1374delinsGAA
ENST00000557921.3:c.*4_*6delinsGAA	ENSP00000453157.3:n.*4_*6delinsGAA
ENST00000699682.1:n.1459_1461delinsGAA
ENST00000699683.1:n.1509_1511delinsGAA
ENST00000699684.1:c.*662_*664delinsGAA	ENSP00000514523.1:n.*662_*664delinsGAA
ENST00000699685.1:n.1273_1275delinsGAA
ENST00000699686.1:c.*4_*6delinsGAA	ENSP00000514524.1:n.*4_*6delinsGAA
ENST00000699687.1:c.*4_*6delinsGAA	ENSP00000514525.1:n.*4_*6delinsGAA
ENST00000699688.1:n.1269_1271delinsGAA
ENST00000699689.1:n.1625_1627delinsGAA
ENST00000699690.1:n.1822_1824delinsGAA
ENST00000699691.1:n.1966_1968delinsGAA
ENST00000699693.1:n.1478+8_1478+10delinsGAA
ENST00000699694.1:n.1728_1730delinsGAA
ENST00000699695.1:c.*433+8_*433+10delinsGAA	ENSP00000514526.1:n.*433+8_*433+10delinsGAA
ENST00000699696.1:n.1372_1374delinsGAA
ENST00000699697.1:c.1061+8_1061+10delinsGAA	ENSP00000514527.1:n.1061+8_1061+10delinsGAA
ENST00000699698.1:n.982+8_982+10delinsGAA
ENST00000699699.1:n.1393_1395delinsGAA
ENST00000699700.1:n.1516_1518delinsGAA
ENST00000699701.1:c.*449_*451delinsGAA	ENSP00000514528.1:n.*449_*451delinsGAA
ENST00000267415.12:c.1061+8_1061+10delinsGAA MANE Select	ENSP00000267415.7:n.1061+8_1061+10delinsGAA
ENST00000646753.1:c.956+8_956+10delinsGAA	ENSP00000494065.1:n.956+8_956+10delinsGAA
ENST00000267415.11:c.1061+8_1061+10delinsGAA	ENSP00000267415.7:n.1061+8_1061+10delinsGAA
ENST00000399423.8:c.*4_*6delinsGAA	ENSP00000382350.4:n.*4_*6delinsGAA
ENST00000557915.1:n.188_190delinsGAA
ENST00000558566.1:c.*441_*443delinsGAA	ENSP00000453025.1:n.*441_*443delinsGAA
ENST00000559969.5:c.827_829delinsGAA
ENST00000560019.5:c.56+8_56+10delinsGAA	ENSP00000453113.1:n.56+8_56+10delinsGAA
ENST00000626689.2:c.*433+8_*433+10delinsGAA	ENSP00000486681.1:n.*433+8_*433+10delinsGAA
NM_001099274.1:c.1061+8_1061+10delinsGAA	NP_001092744.1:n.1061+8_1061+10delinsGAA
NM_012461.2:c.*4_*6delinsGAA	NP_036593.2:n.*4_*6delinsGAA
XM_005267528.2:c.1061+8_1061+10delinsGAA	XP_005267585.1:n.1061+8_1061+10delinsGAA
XM_005267529.2:c.956+8_956+10delinsGAA	XP_005267586.1:n.956+8_956+10delinsGAA
NM_001099274.2:c.1061+8_1061+10delinsGAA	NP_001092744.1:n.1061+8_1061+10delinsGAA
NM_001363668.1:c.956+8_956+10delinsGAA	NP_001350597.1:n.956+8_956+10delinsGAA
NM_012461.3:c.*4_*6delinsGAA	NP_036593.2:n.*4_*6delinsGAA
XM_011536642.2:c.*449_*451delinsGAA	XP_011534944.1:n.*449_*451delinsGAA
XM_017021216.2:c.419+8_419+10delinsGAA	XP_016876705.1:n.419+8_419+10delinsGAA
XM_017021217.1:c.419+8_419+10delinsGAA	XP_016876706.1:n.419+8_419+10delinsGAA
NM_001099274.3:c.1061+8_1061+10delinsGAA MANE Select	NP_001092744.1:n.1061+8_1061+10delinsGAA
NM_001363668.2:c.956+8_956+10delinsGAA	NP_001350597.1:n.956+8_956+10delinsGAA