Canonical Allele Identifier: CA2123849045

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240367_24240372delinsGAAGGC , CM000676.2:g.24240367_24240372delinsGAAGGC	GRCh38
NC_000014.8:g.24709573_24709578delinsGAAGGC , CM000676.1:g.24709573_24709578delinsGAAGGC	GRCh37
NC_000014.7:g.23779413_23779418delinsGAAGGC	NCBI36
NG_016650.1:g.7303_7308delinsGCCTTC
NG_054634.1:g.12951_12956delinsGAAGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1411_1416delinsGCCTTC
ENST00000557921.3:c.*43_*48delinsGCCTTC	ENSP00000453157.3:n.*43_*48delinsGCCTTC
ENST00000699682.1:n.1498_1503delinsGCCTTC
ENST00000699683.1:n.1548_1553delinsGCCTTC
ENST00000699684.1:c.*701_*706delinsGCCTTC	ENSP00000514523.1:n.*701_*706delinsGCCTTC
ENST00000699685.1:n.1312_1317delinsGCCTTC
ENST00000699686.1:c.*43_*48delinsGCCTTC	ENSP00000514524.1:n.*43_*48delinsGCCTTC
ENST00000699687.1:c.*43_*48delinsGCCTTC	ENSP00000514525.1:n.*43_*48delinsGCCTTC
ENST00000699688.1:n.1308_1313delinsGCCTTC
ENST00000699689.1:n.1664_1669delinsGCCTTC
ENST00000699690.1:n.1861_1866delinsGCCTTC
ENST00000699691.1:n.2005_2010delinsGCCTTC
ENST00000699693.1:n.1479-42_1479-37delinsGCCTTC
ENST00000699694.1:n.1767_1772delinsGCCTTC
ENST00000699695.1:c.*434-42_*434-37delinsGCCTTC	ENSP00000514526.1:n.*434-42_*434-37delinsGCCTTC
ENST00000699696.1:n.1411_1416delinsGCCTTC
ENST00000699697.1:c.1062-42_1062-37delinsGCCTTC	ENSP00000514527.1:n.1062-42_1062-37delinsGCCTTC
ENST00000699698.1:n.983-42_983-37delinsGCCTTC
ENST00000699699.1:n.1432_1437delinsGCCTTC
ENST00000699700.1:n.1555_1560delinsGCCTTC
ENST00000699701.1:c.*488_*493delinsGCCTTC	ENSP00000514528.1:n.*488_*493delinsGCCTTC
ENST00000267415.12:c.1062-42_1062-37delinsGCCTTC MANE Select	ENSP00000267415.7:n.1062-42_1062-37delinsGCCTTC
ENST00000646753.1:c.957-42_957-37delinsGCCTTC	ENSP00000494065.1:n.957-42_957-37delinsGCCTTC
ENST00000267415.11:c.1062-42_1062-37delinsGCCTTC	ENSP00000267415.7:n.1062-42_1062-37delinsGCCTTC
ENST00000399423.8:c.*43_*48delinsGCCTTC	ENSP00000382350.4:n.*43_*48delinsGCCTTC
ENST00000557915.1:n.227_232delinsGCCTTC
ENST00000558566.1:c.*480_*485delinsGCCTTC	ENSP00000453025.1:n.*480_*485delinsGCCTTC
ENST00000559969.5:c.866_871delinsGCCTTC
ENST00000560019.5:c.57-42_57-37delinsGCCTTC	ENSP00000453113.1:n.57-42_57-37delinsGCCTTC
ENST00000626689.2:c.*434-42_*434-37delinsGCCTTC	ENSP00000486681.1:n.*434-42_*434-37delinsGCCTTC
NM_001099274.1:c.1062-42_1062-37delinsGCCTTC	NP_001092744.1:n.1062-42_1062-37delinsGCCTTC
NM_012461.2:c.*43_*48delinsGCCTTC	NP_036593.2:n.*43_*48delinsGCCTTC
XM_005267528.2:c.1062-42_1062-37delinsGCCTTC	XP_005267585.1:n.1062-42_1062-37delinsGCCTTC
XM_005267529.2:c.957-42_957-37delinsGCCTTC	XP_005267586.1:n.957-42_957-37delinsGCCTTC
NM_001099274.2:c.1062-42_1062-37delinsGCCTTC	NP_001092744.1:n.1062-42_1062-37delinsGCCTTC
NM_001363668.1:c.957-42_957-37delinsGCCTTC	NP_001350597.1:n.957-42_957-37delinsGCCTTC
NM_012461.3:c.*43_*48delinsGCCTTC	NP_036593.2:n.*43_*48delinsGCCTTC
XM_011536642.2:c.*488_*493delinsGCCTTC	XP_011534944.1:n.*488_*493delinsGCCTTC
XM_017021216.2:c.420-42_420-37delinsGCCTTC	XP_016876705.1:n.420-42_420-37delinsGCCTTC
XM_017021217.1:c.420-42_420-37delinsGCCTTC	XP_016876706.1:n.420-42_420-37delinsGCCTTC
NM_001099274.3:c.1062-42_1062-37delinsGCCTTC MANE Select	NP_001092744.1:n.1062-42_1062-37delinsGCCTTC
NM_001363668.2:c.957-42_957-37delinsGCCTTC	NP_001350597.1:n.957-42_957-37delinsGCCTTC