Canonical Allele Identifier: CA7130508

Gene: TINF2

Linked Data

• dbSNP Id: rs532494516
• ExAC: 14:24709557 G / A
• gnomAD v2: 14-24709557-G-A
• gnomAD v4: 14-24240351-G-A
• MyVariant Identifiers: chr14:g.24709557G>A (hg19) ; chr14:g.24240351G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240351G>A , CM000676.2:g.24240351G>A	GRCh38
NC_000014.8:g.24709557G>A , CM000676.1:g.24709557G>A	GRCh37
NC_000014.7:g.23779397G>A	NCBI36
NG_016650.1:g.7324C>T
NG_054634.1:g.12935G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1432C>T
ENST00000557921.3:c.*64C>T	ENSP00000453157.3:n.*64C>T
ENST00000699682.1:n.1519C>T
ENST00000699683.1:n.1569C>T
ENST00000699684.1:c.*722C>T	ENSP00000514523.1:n.*722C>T
ENST00000699685.1:n.1333C>T
ENST00000699686.1:c.*64C>T	ENSP00000514524.1:n.*64C>T
ENST00000699687.1:c.*64C>T	ENSP00000514525.1:n.*64C>T
ENST00000699688.1:n.1329C>T
ENST00000699689.1:n.1685C>T
ENST00000699690.1:n.1882C>T
ENST00000699691.1:n.2026C>T
ENST00000699693.1:n.1479-21C>T
ENST00000699694.1:n.1788C>T
ENST00000699695.1:c.*434-21C>T	ENSP00000514526.1:n.*434-21C>T
ENST00000699696.1:n.1432C>T
ENST00000699697.1:c.1062-21C>T	ENSP00000514527.1:n.1062-21C>T
ENST00000699698.1:n.983-21C>T
ENST00000699699.1:n.1453C>T
ENST00000699700.1:n.1576C>T
ENST00000699701.1:c.*509C>T	ENSP00000514528.1:n.*509C>T
ENST00000267415.12:c.1062-21C>T MANE Select	ENSP00000267415.7:n.1062-21C>T
ENST00000646753.1:c.957-21C>T	ENSP00000494065.1:n.957-21C>T
ENST00000267415.11:c.1062-21C>T	ENSP00000267415.7:n.1062-21C>T
ENST00000399423.8:c.*64C>T	ENSP00000382350.4:n.*64C>T
ENST00000557915.1:n.248C>T
ENST00000558566.1:c.*501C>T	ENSP00000453025.1:n.*501C>T
ENST00000559969.5:c.887C>T
ENST00000560019.5:c.57-21C>T	ENSP00000453113.1:n.57-21C>T
ENST00000626689.2:c.*434-21C>T	ENSP00000486681.1:n.*434-21C>T
NM_001099274.1:c.1062-21C>T	NP_001092744.1:n.1062-21C>T
NM_012461.2:c.*64C>T	NP_036593.2:n.*64C>T
XM_005267528.2:c.1062-21C>T	XP_005267585.1:n.1062-21C>T
XM_005267529.2:c.957-21C>T	XP_005267586.1:n.957-21C>T
NM_001099274.2:c.1062-21C>T	NP_001092744.1:n.1062-21C>T
NM_001363668.1:c.957-21C>T	NP_001350597.1:n.957-21C>T
NM_012461.3:c.*64C>T	NP_036593.2:n.*64C>T
XM_011536642.2:c.*509C>T	XP_011534944.1:n.*509C>T
XM_017021216.2:c.420-21C>T	XP_016876705.1:n.420-21C>T
XM_017021217.1:c.420-21C>T	XP_016876706.1:n.420-21C>T
NM_001099274.3:c.1062-21C>T MANE Select	NP_001092744.1:n.1062-21C>T
NM_001363668.2:c.957-21C>T	NP_001350597.1:n.957-21C>T