Canonical Allele Identifier: CA257880859

Gene: TINF2

Linked Data

• dbSNP Id: rs907499675
• gnomAD v2: 14-24709582-CA-C
• gnomAD v3: 14-24240376-CA-C
• gnomAD v4: 14-24240376-CA-C
• MyVariant Identifiers: chr14:g.24709583del (hg19) ; chr14:g.24240377del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240379del , CM000676.2:g.24240379del	GRCh38
NC_000014.8:g.24709585del , CM000676.1:g.24709585del	GRCh37
NC_000014.7:g.23779425del	NCBI36
NG_016650.1:g.7298del
NG_054634.1:g.12963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1406del
ENST00000557921.3:c.*38del	ENSP00000453157.3:n.*38del
ENST00000699682.1:n.1493del
ENST00000699683.1:n.1543del
ENST00000699684.1:c.*696del	ENSP00000514523.1:n.*696del
ENST00000699685.1:n.1307del
ENST00000699686.1:c.*38del	ENSP00000514524.1:n.*38del
ENST00000699687.1:c.*38del	ENSP00000514525.1:n.*38del
ENST00000699688.1:n.1303del
ENST00000699689.1:n.1659del
ENST00000699690.1:n.1856del
ENST00000699691.1:n.2000del
ENST00000699693.1:n.1478+42del
ENST00000699694.1:n.1762del
ENST00000699695.1:c.*433+42del	ENSP00000514526.1:n.*433+42del
ENST00000699696.1:n.1406del
ENST00000699697.1:c.1061+42del	ENSP00000514527.1:n.1061+42del
ENST00000699698.1:n.982+42del
ENST00000699699.1:n.1427del
ENST00000699700.1:n.1550del
ENST00000699701.1:c.*483del	ENSP00000514528.1:n.*483del
ENST00000267415.12:c.1061+42del MANE Select	ENSP00000267415.7:n.1061+42del
ENST00000646753.1:c.956+42del	ENSP00000494065.1:n.956+42del
ENST00000267415.11:c.1061+42del	ENSP00000267415.7:n.1061+42del
ENST00000399423.8:c.*38del	ENSP00000382350.4:n.*38del
ENST00000557915.1:n.222del
ENST00000558566.1:c.*475del	ENSP00000453025.1:n.*475del
ENST00000559969.5:c.861del
ENST00000560019.5:c.56+42del	ENSP00000453113.1:n.56+42del
ENST00000626689.2:c.*433+42del	ENSP00000486681.1:n.*433+42del
NM_001099274.1:c.1061+42del	NP_001092744.1:n.1061+42del
NM_012461.2:c.*38del	NP_036593.2:n.*38del
XM_005267528.2:c.1061+42del	XP_005267585.1:n.1061+42del
XM_005267529.2:c.956+42del	XP_005267586.1:n.956+42del
NM_001099274.2:c.1061+42del	NP_001092744.1:n.1061+42del
NM_001363668.1:c.956+42del	NP_001350597.1:n.956+42del
NM_012461.3:c.*38del	NP_036593.2:n.*38del
XM_011536642.2:c.*483del	XP_011534944.1:n.*483del
XM_017021216.2:c.419+42del	XP_016876705.1:n.419+42del
XM_017021217.1:c.419+42del	XP_016876706.1:n.419+42del
NM_001099274.3:c.1061+42del MANE Select	NP_001092744.1:n.1061+42del
NM_001363668.2:c.956+42del	NP_001350597.1:n.956+42del