Canonical Allele Identifier: CA613320519

Gene: TINF2

Linked Data

• dbSNP Id: rs1566366283
• gnomAD v2: 14-24709557-G-GAT
• gnomAD v4: 14-24240351-G-GAT
• MyVariant Identifiers: chr14:g.24709557_24709558insAT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240352_24240353insTA , CM000676.2:g.24240352_24240353insTA	GRCh38
NC_000014.8:g.24709558_24709559insTA , CM000676.1:g.24709558_24709559insTA	GRCh37
NC_000014.7:g.23779398_23779399insTA	NCBI36
NG_016650.1:g.7323_7324insAT
NG_054634.1:g.12936_12937insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1431_1432insAT
ENST00000557921.3:c.*63_*64insAT	ENSP00000453157.3:n.*63_*64insAT
ENST00000699682.1:n.1518_1519insAT
ENST00000699683.1:n.1568_1569insAT
ENST00000699684.1:c.*721_*722insAT	ENSP00000514523.1:n.*721_*722insAT
ENST00000699685.1:n.1332_1333insAT
ENST00000699686.1:c.*63_*64insAT	ENSP00000514524.1:n.*63_*64insAT
ENST00000699687.1:c.*63_*64insAT	ENSP00000514525.1:n.*63_*64insAT
ENST00000699688.1:n.1328_1329insAT
ENST00000699689.1:n.1684_1685insAT
ENST00000699690.1:n.1881_1882insAT
ENST00000699691.1:n.2025_2026insAT
ENST00000699693.1:n.1479-22_1479-21insAT
ENST00000699694.1:n.1787_1788insAT
ENST00000699695.1:c.*434-22_*434-21insAT	ENSP00000514526.1:n.*434-22_*434-21insAT
ENST00000699696.1:n.1431_1432insAT
ENST00000699697.1:c.1062-22_1062-21insAT	ENSP00000514527.1:n.1062-22_1062-21insAT
ENST00000699698.1:n.983-22_983-21insAT
ENST00000699699.1:n.1452_1453insAT
ENST00000699700.1:n.1575_1576insAT
ENST00000699701.1:c.*508_*509insAT	ENSP00000514528.1:n.*508_*509insAT
ENST00000267415.12:c.1062-22_1062-21insAT MANE Select	ENSP00000267415.7:n.1062-22_1062-21insAT
ENST00000646753.1:c.957-22_957-21insAT	ENSP00000494065.1:n.957-22_957-21insAT
ENST00000267415.11:c.1062-22_1062-21insAT	ENSP00000267415.7:n.1062-22_1062-21insAT
ENST00000399423.8:c.*63_*64insAT	ENSP00000382350.4:n.*63_*64insAT
ENST00000557915.1:n.247_248insAT
ENST00000558566.1:c.*500_*501insAT	ENSP00000453025.1:n.*500_*501insAT
ENST00000559969.5:c.886_887insAT
ENST00000560019.5:c.57-22_57-21insAT	ENSP00000453113.1:n.57-22_57-21insAT
ENST00000626689.2:c.*434-22_*434-21insAT	ENSP00000486681.1:n.*434-22_*434-21insAT
NM_001099274.1:c.1062-22_1062-21insAT	NP_001092744.1:n.1062-22_1062-21insAT
NM_012461.2:c.*63_*64insAT	NP_036593.2:n.*63_*64insAT
XM_005267528.2:c.1062-22_1062-21insAT	XP_005267585.1:n.1062-22_1062-21insAT
XM_005267529.2:c.957-22_957-21insAT	XP_005267586.1:n.957-22_957-21insAT
NM_001099274.2:c.1062-22_1062-21insAT	NP_001092744.1:n.1062-22_1062-21insAT
NM_001363668.1:c.957-22_957-21insAT	NP_001350597.1:n.957-22_957-21insAT
NM_012461.3:c.*63_*64insAT	NP_036593.2:n.*63_*64insAT
XM_011536642.2:c.*508_*509insAT	XP_011534944.1:n.*508_*509insAT
XM_017021216.2:c.420-22_420-21insAT	XP_016876705.1:n.420-22_420-21insAT
XM_017021217.1:c.420-22_420-21insAT	XP_016876706.1:n.420-22_420-21insAT
NM_001099274.3:c.1062-22_1062-21insAT MANE Select	NP_001092744.1:n.1062-22_1062-21insAT
NM_001363668.2:c.957-22_957-21insAT	NP_001350597.1:n.957-22_957-21insAT