Canonical Allele Identifier: CA364494346

Gene: TINAG

Linked Data

• dbSNP Id: rs1058768
• MyVariant Identifiers: chr6:g.54186147T>A (hg19) ; chr6:g.54321349T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.54321349T>A , CM000668.2:g.54321349T>A	GRCh38
NC_000006.11:g.54186147T>A , CM000668.1:g.54186147T>A	GRCh37
NC_000006.10:g.54294106T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000259782.9:c.472T>A MANE Select	ENSP00000259782.4:p.Ser158Thr
ENST00000259782.8:c.472T>A	ENSP00000259782.4:p.Ser158Thr
ENST00000370864.3:c.418T>A	ENSP00000359901.3:p.Ser140Thr
ENST00000370869.7:c.460T>A	ENSP00000359906.3:p.Ser154Thr
ENST00000486436.1:n.534T>A
NM_014464.3:c.472T>A	NP_055279.3:p.Ser158Thr
XM_006715061.2:c.481T>A	XP_006715124.1:p.Ser161Thr
XM_006715062.2:c.418T>A	XP_006715125.1:p.Ser140Thr
XM_006715063.2:c.481T>A	XP_006715126.1:p.Ser161Thr
XM_011514496.1:c.365-5449T>A	XP_011512798.1:n.365-5449T>A
XM_011514497.1:c.356-5449T>A	XP_011512799.1:n.356-5449T>A
XM_011514498.1:c.256T>A	XP_011512800.1:p.Ser86Thr
XM_011514499.1:c.140-5449T>A	XP_011512801.1:n.140-5449T>A
XR_427828.2:n.514T>A
XM_011514497.2:c.356-5449T>A	XP_011512799.1:n.356-5449T>A
XM_017010745.1:c.472T>A	XP_016866234.1:p.Ser158Thr
XM_017010746.1:c.247T>A	XP_016866235.1:p.Ser83Thr
XM_017010747.1:c.131-5449T>A	XP_016866236.1:n.131-5449T>A
XM_017010748.1:c.-34T>A	XP_016866237.1:n.-34T>A
XR_001743344.2:n.582T>A
NM_014464.4:c.472T>A MANE Select	NP_055279.3:p.Ser158Thr