Canonical Allele Identifier: CA7130566

Gene: TINF2

Linked Data

• dbSNP Id: rs768311481
• ExAC: 14:24709932 G / A
• gnomAD v2: 14-24709932-G-A
• gnomAD v4: 14-24240726-G-A
• MyVariant Identifiers: chr14:g.24709932G>A (hg19) ; chr14:g.24240726G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240726G>A , CM000676.2:g.24240726G>A	GRCh38
NC_000014.8:g.24709932G>A , CM000676.1:g.24709932G>A	GRCh37
NC_000014.7:g.23779772G>A	NCBI36
NG_016650.1:g.6949C>T
NG_054634.1:g.13310G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1057C>T
ENST00000557921.3:c.646C>T	ENSP00000453157.3:p.Pro216Ser
ENST00000699682.1:n.1144C>T
ENST00000699683.1:n.1194C>T
ENST00000699684.1:c.*347C>T	ENSP00000514523.1:n.*347C>T
ENST00000699685.1:n.958C>T
ENST00000699686.1:c.547C>T	ENSP00000514524.1:p.Pro183Ser
ENST00000699687.1:c.649C>T	ENSP00000514525.1:p.Pro217Ser
ENST00000699688.1:n.954C>T
ENST00000699689.1:n.1310C>T
ENST00000699690.1:n.1507C>T
ENST00000699691.1:n.1651C>T
ENST00000699693.1:n.1171C>T
ENST00000699694.1:n.1413C>T
ENST00000699695.1:c.*126C>T	ENSP00000514526.1:n.*126C>T
ENST00000699696.1:n.1057C>T
ENST00000699697.1:c.754C>T	ENSP00000514527.1:p.Pro252Ser
ENST00000699698.1:n.675C>T
ENST00000699699.1:n.1078C>T
ENST00000699700.1:n.1201C>T
ENST00000699701.1:c.*134C>T	ENSP00000514528.1:n.*134C>T
ENST00000267415.12:c.754C>T MANE Select	ENSP00000267415.7:p.Pro252Ser
ENST00000557921.2:c.646C>T	ENSP00000453157.2:p.Pro216Ser
ENST00000646753.1:c.649C>T	ENSP00000494065.1:p.Pro217Ser
ENST00000267415.11:c.754C>T	ENSP00000267415.7:p.Pro252Ser
ENST00000399423.8:c.754C>T	ENSP00000382350.4:p.Pro252Ser
ENST00000558476.5:c.316C>T	ENSP00000452724.1:p.Pro106Ser
ENST00000558566.1:c.*126C>T	ENSP00000453025.1:n.*126C>T
ENST00000559019.1:c.*126C>T	ENSP00000453675.1:n.*126C>T
ENST00000559549.1:n.480C>T
ENST00000559969.5:c.710C>T
ENST00000626689.2:c.*126C>T	ENSP00000486681.1:n.*126C>T
NM_001099274.1:c.754C>T	NP_001092744.1:p.Pro252Ser
NM_012461.2:c.754C>T	NP_036593.2:p.Pro252Ser
XM_005267528.2:c.754C>T	XP_005267585.1:p.Pro252Ser
XM_005267529.2:c.649C>T	XP_005267586.1:p.Pro217Ser
NM_001099274.2:c.754C>T	NP_001092744.1:p.Pro252Ser
NM_001363668.1:c.649C>T	NP_001350597.1:p.Pro217Ser
NM_012461.3:c.754C>T	NP_036593.2:p.Pro252Ser
XM_011536642.2:c.*134C>T	XP_011534944.1:n.*134C>T
XM_017021216.2:c.112C>T	XP_016876705.1:p.Pro38Ser
XM_017021217.1:c.112C>T	XP_016876706.1:p.Pro38Ser
NM_001099274.3:c.754C>T MANE Select	NP_001092744.1:p.Pro252Ser
NM_001363668.2:c.649C>T	NP_001350597.1:p.Pro217Ser