Canonical Allele Identifier: CA12324106

Gene: SUPT3H

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44978769T>A , CM000668.2:g.44978769T>A	GRCh38
NC_000006.11:g.44946506T>A , CM000668.1:g.44946506T>A	GRCh37
NC_000006.10:g.45054484T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371459.6:c.505-16941A>T MANE Select	ENSP00000360514.1:n.505-16941A>T
ENST00000637763.2:c.319-16941A>T	ENSP00000490652.2:n.319-16941A>T
ENST00000674231.1:c.406-16941A>T	ENSP00000501386.1:n.406-16941A>T
ENST00000306867.9:c.49-16941A>T	ENSP00000306718.6:n.49-16941A>T
ENST00000371459.5:c.505-16941A>T	ENSP00000360514.1:n.505-16941A>T
ENST00000371460.5:c.538-16941A>T	ENSP00000360515.1:n.538-16941A>T
ENST00000475057.5:c.505-16941A>T	ENSP00000436411.1:n.505-16941A>T
NM_001261823.1:c.49-16941A>T	NP_001248752.1:n.49-16941A>T
NM_003599.3:c.505-16941A>T	NP_003590.1:n.505-16941A>T
NM_181356.2:c.538-16941A>T	NP_852001.1:n.538-16941A>T
XM_011514949.1:c.538-16941A>T	XP_011513251.1:n.538-16941A>T
XM_011514950.1:c.505-16941A>T	XP_011513252.1:n.505-16941A>T
XM_011514951.1:c.505-16941A>T	XP_011513253.1:n.505-16941A>T
XM_011514952.1:c.505-16941A>T	XP_011513254.1:n.505-16941A>T
XM_011514953.1:c.505-16941A>T	XP_011513255.1:n.505-16941A>T
XM_011514954.1:c.505-16941A>T	XP_011513256.1:n.505-16941A>T
XM_011514955.1:c.538-16941A>T	XP_011513257.1:n.538-16941A>T
XR_926319.1:n.589-16941A>T
XR_926320.1:n.589-16941A>T
XR_926321.1:n.589-16941A>T
NM_001350324.1:c.505-16941A>T	NP_001337253.1:n.505-16941A>T
NM_001350325.1:c.499-16941A>T	NP_001337254.1:n.499-16941A>T
NM_001350326.1:c.442-16941A>T	NP_001337255.1:n.442-16941A>T
NM_001350327.1:c.247-16941A>T	NP_001337256.1:n.247-16941A>T
NM_001350329.1:c.505-16941A>T	NP_001337258.1:n.505-16941A>T
NR_146632.1:n.602-16941A>T
NR_146633.1:n.664-16941A>T
NR_146634.1:n.616-16941A>T
NR_146635.1:n.520-16941A>T
XM_011514949.3:c.538-16941A>T	XP_011513251.1:n.538-16941A>T
XM_011514951.3:c.505-16941A>T	XP_011513253.1:n.505-16941A>T
XM_011514952.2:c.505-16941A>T	XP_011513254.1:n.505-16941A>T
XM_011514953.3:c.505-16941A>T	XP_011513255.1:n.505-16941A>T
XM_011514954.3:c.505-16941A>T	XP_011513256.1:n.505-16941A>T
XM_017011369.2:c.538-16941A>T	XP_016866858.1:n.538-16941A>T
XM_017011370.1:c.538-16941A>T	XP_016866859.1:n.538-16941A>T
XM_017011371.1:c.505-16941A>T	XP_016866860.1:n.505-16941A>T
XM_017011374.2:c.247-16941A>T	XP_016866863.1:n.247-16941A>T
XM_024446572.1:c.505-16941A>T	XP_024302340.1:n.505-16941A>T
XR_001743685.1:n.589-16941A>T
XR_001743688.1:n.589-16941A>T
XR_001743691.1:n.789-16941A>T
XR_001743692.1:n.789-16941A>T
XR_002956310.1:n.789-16941A>T
XR_926319.3:n.589-16941A>T
NM_003599.4:c.505-16941A>T MANE Select	NP_003590.1:n.505-16941A>T
NM_001261823.2:c.49-16941A>T	NP_001248752.1:n.49-16941A>T
NM_001350324.2:c.505-16941A>T	NP_001337253.1:n.505-16941A>T
NM_001350325.2:c.499-16941A>T	NP_001337254.1:n.499-16941A>T
NM_001350326.2:c.442-16941A>T	NP_001337255.1:n.442-16941A>T
NM_001350327.2:c.247-16941A>T	NP_001337256.1:n.247-16941A>T
NM_001350329.2:c.505-16941A>T	NP_001337258.1:n.505-16941A>T
NM_181356.3:c.538-16941A>T	NP_852001.1:n.538-16941A>T
NR_146632.2:n.672-16941A>T
NR_146634.2:n.658-16941A>T
NR_146635.2:n.664-16941A>T