Canonical Allele Identifier: CA389223585

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709657G>C (hg19) ; chr14:g.24240451G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240451G>C , CM000676.2:g.24240451G>C	GRCh38
NC_000014.8:g.24709657G>C , CM000676.1:g.24709657G>C	GRCh37
NC_000014.7:g.23779497G>C	NCBI36
NG_016650.1:g.7224C>G
NG_054634.1:g.13035G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1332C>G
ENST00000557921.3:c.921C>G	ENSP00000453157.3:p.Asn307Lys
ENST00000699682.1:n.1419C>G
ENST00000699683.1:n.1469C>G
ENST00000699684.1:c.*622C>G	ENSP00000514523.1:n.*622C>G
ENST00000699685.1:n.1233C>G
ENST00000699686.1:c.822C>G	ENSP00000514524.1:p.Asn274Lys
ENST00000699687.1:c.924C>G	ENSP00000514525.1:p.Asn308Lys
ENST00000699688.1:n.1229C>G
ENST00000699689.1:n.1585C>G
ENST00000699690.1:n.1782C>G
ENST00000699691.1:n.1926C>G
ENST00000699693.1:n.1446C>G
ENST00000699694.1:n.1688C>G
ENST00000699695.1:c.*401C>G	ENSP00000514526.1:n.*401C>G
ENST00000699696.1:n.1332C>G
ENST00000699697.1:c.1029C>G	ENSP00000514527.1:p.Asn343Lys
ENST00000699698.1:n.950C>G
ENST00000699699.1:n.1353C>G
ENST00000699700.1:n.1476C>G
ENST00000699701.1:c.*409C>G	ENSP00000514528.1:n.*409C>G
ENST00000267415.12:c.1029C>G MANE Select	ENSP00000267415.7:p.Asn343Lys
ENST00000646753.1:c.924C>G	ENSP00000494065.1:p.Asn308Lys
ENST00000267415.11:c.1029C>G	ENSP00000267415.7:p.Asn343Lys
ENST00000399423.8:c.1029C>G	ENSP00000382350.4:p.Asn343Lys
ENST00000557915.1:n.148C>G
ENST00000558566.1:c.*401C>G	ENSP00000453025.1:n.*401C>G
ENST00000559969.5:c.787C>G
ENST00000560019.5:c.24C>G	ENSP00000453113.1:p.Asn8Lys
ENST00000626689.2:c.*401C>G	ENSP00000486681.1:n.*401C>G
NM_001099274.1:c.1029C>G	NP_001092744.1:p.Asn343Lys
NM_012461.2:c.1029C>G	NP_036593.2:p.Asn343Lys
XM_005267528.2:c.1029C>G	XP_005267585.1:p.Asn343Lys
XM_005267529.2:c.924C>G	XP_005267586.1:p.Asn308Lys
NM_001099274.2:c.1029C>G	NP_001092744.1:p.Asn343Lys
NM_001363668.1:c.924C>G	NP_001350597.1:p.Asn308Lys
NM_012461.3:c.1029C>G	NP_036593.2:p.Asn343Lys
XM_011536642.2:c.*409C>G	XP_011534944.1:n.*409C>G
XM_017021216.2:c.387C>G	XP_016876705.1:p.Asn129Lys
XM_017021217.1:c.387C>G	XP_016876706.1:p.Asn129Lys
NM_001099274.3:c.1029C>G MANE Select	NP_001092744.1:p.Asn343Lys
NM_001363668.2:c.924C>G	NP_001350597.1:p.Asn308Lys