Canonical Allele Identifier: CA2123849056

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240376_24240377delinsCA , CM000676.2:g.24240376_24240377delinsCA	GRCh38
NC_000014.8:g.24709582_24709583delinsCA , CM000676.1:g.24709582_24709583delinsCA	GRCh37
NC_000014.7:g.23779422_23779423delinsCA	NCBI36
NG_016650.1:g.7298_7299delinsTG
NG_054634.1:g.12960_12961delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1406_1407delinsTG
ENST00000557921.3:c.*38_*39delinsTG	ENSP00000453157.3:n.*38_*39delinsTG
ENST00000699682.1:n.1493_1494delinsTG
ENST00000699683.1:n.1543_1544delinsTG
ENST00000699684.1:c.*696_*697delinsTG	ENSP00000514523.1:n.*696_*697delinsTG
ENST00000699685.1:n.1307_1308delinsTG
ENST00000699686.1:c.*38_*39delinsTG	ENSP00000514524.1:n.*38_*39delinsTG
ENST00000699687.1:c.*38_*39delinsTG	ENSP00000514525.1:n.*38_*39delinsTG
ENST00000699688.1:n.1303_1304delinsTG
ENST00000699689.1:n.1659_1660delinsTG
ENST00000699690.1:n.1856_1857delinsTG
ENST00000699691.1:n.2000_2001delinsTG
ENST00000699693.1:n.1478+42_1478+43delinsTG
ENST00000699694.1:n.1762_1763delinsTG
ENST00000699695.1:c.*433+42_*433+43delinsTG	ENSP00000514526.1:n.*433+42_*433+43delinsTG
ENST00000699696.1:n.1406_1407delinsTG
ENST00000699697.1:c.1061+42_1061+43delinsTG	ENSP00000514527.1:n.1061+42_1061+43delinsTG
ENST00000699698.1:n.982+42_982+43delinsTG
ENST00000699699.1:n.1427_1428delinsTG
ENST00000699700.1:n.1550_1551delinsTG
ENST00000699701.1:c.*483_*484delinsTG	ENSP00000514528.1:n.*483_*484delinsTG
ENST00000267415.12:c.1061+42_1061+43delinsTG MANE Select	ENSP00000267415.7:n.1061+42_1061+43delinsTG
ENST00000646753.1:c.956+42_956+43delinsTG	ENSP00000494065.1:n.956+42_956+43delinsTG
ENST00000267415.11:c.1061+42_1061+43delinsTG	ENSP00000267415.7:n.1061+42_1061+43delinsTG
ENST00000399423.8:c.*38_*39delinsTG	ENSP00000382350.4:n.*38_*39delinsTG
ENST00000557915.1:n.222_223delinsTG
ENST00000558566.1:c.*475_*476delinsTG	ENSP00000453025.1:n.*475_*476delinsTG
ENST00000559969.5:c.861_862delinsTG
ENST00000560019.5:c.56+42_56+43delinsTG	ENSP00000453113.1:n.56+42_56+43delinsTG
ENST00000626689.2:c.*433+42_*433+43delinsTG	ENSP00000486681.1:n.*433+42_*433+43delinsTG
NM_001099274.1:c.1061+42_1061+43delinsTG	NP_001092744.1:n.1061+42_1061+43delinsTG
NM_012461.2:c.*38_*39delinsTG	NP_036593.2:n.*38_*39delinsTG
XM_005267528.2:c.1061+42_1061+43delinsTG	XP_005267585.1:n.1061+42_1061+43delinsTG
XM_005267529.2:c.956+42_956+43delinsTG	XP_005267586.1:n.956+42_956+43delinsTG
NM_001099274.2:c.1061+42_1061+43delinsTG	NP_001092744.1:n.1061+42_1061+43delinsTG
NM_001363668.1:c.956+42_956+43delinsTG	NP_001350597.1:n.956+42_956+43delinsTG
NM_012461.3:c.*38_*39delinsTG	NP_036593.2:n.*38_*39delinsTG
XM_011536642.2:c.*483_*484delinsTG	XP_011534944.1:n.*483_*484delinsTG
XM_017021216.2:c.419+42_419+43delinsTG	XP_016876705.1:n.419+42_419+43delinsTG
XM_017021217.1:c.419+42_419+43delinsTG	XP_016876706.1:n.419+42_419+43delinsTG
NM_001099274.3:c.1061+42_1061+43delinsTG MANE Select	NP_001092744.1:n.1061+42_1061+43delinsTG
NM_001363668.2:c.956+42_956+43delinsTG	NP_001350597.1:n.956+42_956+43delinsTG