Canonical Allele Identifier: CA13145602

Gene: RSU1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16592300C>T , CM000672.2:g.16592300C>T	GRCh38
NC_000010.10:g.16634299C>T , CM000672.1:g.16634299C>T	GRCh37
NC_000010.9:g.16674305C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345264.10:c.*1094G>A MANE Select	ENSP00000339521.5:n.*1094G>A
ENST00000345264.9:c.*1094G>A	ENSP00000339521.5:n.*1094G>A
ENST00000377921.7:c.*1094G>A	ENSP00000367154.3:n.*1094G>A
ENST00000602389.1:c.*1094G>A	ENSP00000473588.1:n.*1094G>A
NM_012425.3:c.*1094G>A	NP_036557.1:n.*1094G>A
NM_152724.2:c.*1094G>A	NP_689937.2:n.*1094G>A
XM_005252552.4:c.*961G>A	XP_005252609.1:n.*961G>A
NM_012425.4:c.*1094G>A MANE Select	NP_036557.1:n.*1094G>A
NM_152724.3:c.*1094G>A	NP_689937.2:n.*1094G>A