Canonical Allele Identifier: CA12295458

Gene: SUPT3H

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44869619T>G , CM000668.2:g.44869619T>G	GRCh38
NC_000006.11:g.44837356T>G , CM000668.1:g.44837356T>G	GRCh37
NC_000006.10:g.44945334T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371459.6:c.913-39762A>C MANE Select	ENSP00000360514.1:n.913-39762A>C
ENST00000674231.1:c.814-39762A>C	ENSP00000501386.1:n.814-39762A>C
ENST00000306867.9:c.457-39762A>C	ENSP00000306718.6:n.457-39762A>C
ENST00000371458.1:c.262-39743A>C	ENSP00000360513.1:n.262-39743A>C
ENST00000371459.5:c.913-39762A>C	ENSP00000360514.1:n.913-39762A>C
ENST00000371460.5:c.946-39762A>C	ENSP00000360515.1:n.946-39762A>C
ENST00000475057.5:c.913-39762A>C	ENSP00000436411.1:n.913-39762A>C
NM_001261823.1:c.457-39762A>C	NP_001248752.1:n.457-39762A>C
NM_003599.3:c.913-39762A>C	NP_003590.1:n.913-39762A>C
NM_181356.2:c.946-39762A>C	NP_852001.1:n.946-39762A>C
XM_011514949.1:c.*24-39762A>C	XP_011513251.1:n.*24-39762A>C
XM_011514950.1:c.*24-39762A>C	XP_011513252.1:n.*24-39762A>C
XM_011514951.1:c.*24-39762A>C	XP_011513253.1:n.*24-39762A>C
XM_011514952.1:c.*24-39762A>C	XP_011513254.1:n.*24-39762A>C
XM_011514953.1:c.*24-39762A>C	XP_011513255.1:n.*24-39762A>C
XM_011514954.1:c.*24-39762A>C	XP_011513256.1:n.*24-39762A>C
XR_926319.1:n.997-39762A>C
NM_001350324.1:c.*24-39762A>C	NP_001337253.1:n.*24-39762A>C
NM_001350325.1:c.907-39762A>C	NP_001337254.1:n.907-39762A>C
NM_001350326.1:c.850-39762A>C	NP_001337255.1:n.850-39762A>C
NM_001350327.1:c.655-39762A>C	NP_001337256.1:n.655-39762A>C
NM_001350329.1:c.913-39762A>C	NP_001337258.1:n.913-39762A>C
NR_146632.1:n.1010-39762A>C
NR_146633.1:n.1072-39762A>C
NR_146634.1:n.1024-39762A>C
NR_146635.1:n.1069-39762A>C
XM_011514949.3:c.*24-39762A>C	XP_011513251.1:n.*24-39762A>C
XM_011514951.3:c.*24-39762A>C	XP_011513253.1:n.*24-39762A>C
XM_011514952.2:c.*24-39762A>C	XP_011513254.1:n.*24-39762A>C
XM_011514953.3:c.*24-39762A>C	XP_011513255.1:n.*24-39762A>C
XM_011514954.3:c.*24-39762A>C	XP_011513256.1:n.*24-39762A>C
XM_017011369.2:c.*24-39762A>C	XP_016866858.1:n.*24-39762A>C
XM_017011370.1:c.*24-39762A>C	XP_016866859.1:n.*24-39762A>C
XM_017011371.1:c.913-39762A>C	XP_016866860.1:n.913-39762A>C
XM_017011374.2:c.*24-39762A>C	XP_016866863.1:n.*24-39762A>C
XM_024446572.1:c.913-39762A>C	XP_024302340.1:n.913-39762A>C
XR_001743685.1:n.997-39762A>C
XR_001743688.1:n.884-39762A>C
XR_001743691.1:n.1084-39762A>C
XR_002956310.1:n.1338-39762A>C
XR_926319.3:n.997-39762A>C
NM_003599.4:c.913-39762A>C MANE Select	NP_003590.1:n.913-39762A>C
NM_001261823.2:c.457-39762A>C	NP_001248752.1:n.457-39762A>C
NM_001350324.2:c.*24-39762A>C	NP_001337253.1:n.*24-39762A>C
NM_001350325.2:c.907-39762A>C	NP_001337254.1:n.907-39762A>C
NM_001350326.2:c.850-39762A>C	NP_001337255.1:n.850-39762A>C
NM_001350327.2:c.655-39762A>C	NP_001337256.1:n.655-39762A>C
NM_001350329.2:c.913-39762A>C	NP_001337258.1:n.913-39762A>C
NM_181356.3:c.946-39762A>C	NP_852001.1:n.946-39762A>C
NR_146632.2:n.1080-39762A>C
NR_146634.2:n.1066-39762A>C
NR_146635.2:n.1213-39762A>C