Canonical Allele Identifier: CA2561476624

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240244C>G , CM000676.2:g.24240244C>G	GRCh38
NC_000014.8:g.24709450C>G , CM000676.1:g.24709450C>G	GRCh37
NC_000014.7:g.23779290C>G	NCBI36
NG_016650.1:g.7431G>C
NG_054634.1:g.12828C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+19G>C
ENST00000557921.3:c.*171G>C	ENSP00000453157.3:n.*171G>C
ENST00000699682.1:n.1626G>C
ENST00000699683.1:n.1676G>C
ENST00000699684.1:c.*829G>C	ENSP00000514523.1:n.*829G>C
ENST00000699685.1:n.1440G>C
ENST00000699686.1:c.*171G>C	ENSP00000514524.1:n.*171G>C
ENST00000699687.1:c.*171G>C	ENSP00000514525.1:n.*171G>C
ENST00000699688.1:n.1436G>C
ENST00000699689.1:n.1792G>C
ENST00000699690.1:n.1989G>C
ENST00000699691.1:n.2133G>C
ENST00000699692.1:n.68+19G>C
ENST00000699693.1:n.1546+19G>C
ENST00000699694.1:n.1895G>C
ENST00000699695.1:c.*501+19G>C	ENSP00000514526.1:n.*501+19G>C
ENST00000699696.1:n.1520+19G>C
ENST00000699697.1:c.*11G>C	ENSP00000514527.1:n.*11G>C
ENST00000699698.1:n.1069G>C
ENST00000699699.1:n.1560G>C
ENST00000699700.1:n.1683G>C
ENST00000699701.1:c.*616G>C	ENSP00000514528.1:n.*616G>C
ENST00000267415.12:c.1129+19G>C MANE Select	ENSP00000267415.7:n.1129+19G>C
ENST00000646753.1:c.1024+19G>C	ENSP00000494065.1:n.1024+19G>C
ENST00000267415.11:c.1129+19G>C	ENSP00000267415.7:n.1129+19G>C
ENST00000399423.8:c.*171G>C	ENSP00000382350.4:n.*171G>C
ENST00000557915.1:n.336+19G>C
ENST00000558566.1:c.*608G>C	ENSP00000453025.1:n.*608G>C
ENST00000559969.5:c.994G>C
ENST00000560019.5:c.124+19G>C	ENSP00000453113.1:n.124+19G>C
ENST00000626689.2:c.*501+19G>C	ENSP00000486681.1:n.*501+19G>C
NM_001099274.1:c.1129+19G>C	NP_001092744.1:n.1129+19G>C
NM_012461.2:c.*171G>C	NP_036593.2:n.*171G>C
XM_005267528.2:c.1129+19G>C	XP_005267585.1:n.1129+19G>C
XM_005267529.2:c.1024+19G>C	XP_005267586.1:n.1024+19G>C
NM_001099274.2:c.1129+19G>C	NP_001092744.1:n.1129+19G>C
NM_001363668.1:c.1024+19G>C	NP_001350597.1:n.1024+19G>C
NM_012461.3:c.*171G>C	NP_036593.2:n.*171G>C
XM_011536642.2:c.*616G>C	XP_011534944.1:n.*616G>C
XM_017021216.2:c.487+19G>C	XP_016876705.1:n.487+19G>C
XM_017021217.1:c.487+19G>C	XP_016876706.1:n.487+19G>C
NM_001099274.3:c.1129+19G>C MANE Select	NP_001092744.1:n.1129+19G>C
NM_001363668.2:c.1024+19G>C	NP_001350597.1:n.1024+19G>C