Canonical Allele Identifier: CA389223605

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709659T>A (hg19) ; chr14:g.24240453T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240453T>A , CM000676.2:g.24240453T>A	GRCh38
NC_000014.8:g.24709659T>A , CM000676.1:g.24709659T>A	GRCh37
NC_000014.7:g.23779499T>A	NCBI36
NG_016650.1:g.7222A>T
NG_054634.1:g.13037T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1330A>T
ENST00000557921.3:c.919A>T	ENSP00000453157.3:p.Asn307Tyr
ENST00000699682.1:n.1417A>T
ENST00000699683.1:n.1467A>T
ENST00000699684.1:c.*620A>T	ENSP00000514523.1:n.*620A>T
ENST00000699685.1:n.1231A>T
ENST00000699686.1:c.820A>T	ENSP00000514524.1:p.Asn274Tyr
ENST00000699687.1:c.922A>T	ENSP00000514525.1:p.Asn308Tyr
ENST00000699688.1:n.1227A>T
ENST00000699689.1:n.1583A>T
ENST00000699690.1:n.1780A>T
ENST00000699691.1:n.1924A>T
ENST00000699693.1:n.1444A>T
ENST00000699694.1:n.1686A>T
ENST00000699695.1:c.*399A>T	ENSP00000514526.1:n.*399A>T
ENST00000699696.1:n.1330A>T
ENST00000699697.1:c.1027A>T	ENSP00000514527.1:p.Asn343Tyr
ENST00000699698.1:n.948A>T
ENST00000699699.1:n.1351A>T
ENST00000699700.1:n.1474A>T
ENST00000699701.1:c.*407A>T	ENSP00000514528.1:n.*407A>T
ENST00000267415.12:c.1027A>T MANE Select	ENSP00000267415.7:p.Asn343Tyr
ENST00000646753.1:c.922A>T	ENSP00000494065.1:p.Asn308Tyr
ENST00000267415.11:c.1027A>T	ENSP00000267415.7:p.Asn343Tyr
ENST00000399423.8:c.1027A>T	ENSP00000382350.4:p.Asn343Tyr
ENST00000557915.1:n.146A>T
ENST00000558566.1:c.*399A>T	ENSP00000453025.1:n.*399A>T
ENST00000559969.5:c.785A>T
ENST00000560019.5:c.22A>T	ENSP00000453113.1:p.Asn8Tyr
ENST00000626689.2:c.*399A>T	ENSP00000486681.1:n.*399A>T
NM_001099274.1:c.1027A>T	NP_001092744.1:p.Asn343Tyr
NM_012461.2:c.1027A>T	NP_036593.2:p.Asn343Tyr
XM_005267528.2:c.1027A>T	XP_005267585.1:p.Asn343Tyr
XM_005267529.2:c.922A>T	XP_005267586.1:p.Asn308Tyr
NM_001099274.2:c.1027A>T	NP_001092744.1:p.Asn343Tyr
NM_001363668.1:c.922A>T	NP_001350597.1:p.Asn308Tyr
NM_012461.3:c.1027A>T	NP_036593.2:p.Asn343Tyr
XM_011536642.2:c.*407A>T	XP_011534944.1:n.*407A>T
XM_017021216.2:c.385A>T	XP_016876705.1:p.Asn129Tyr
XM_017021217.1:c.385A>T	XP_016876706.1:p.Asn129Tyr
NM_001099274.3:c.1027A>T MANE Select	NP_001092744.1:p.Asn343Tyr
NM_001363668.2:c.922A>T	NP_001350597.1:p.Asn308Tyr