Canonical Allele Identifier: CA1893248077

Gene: RSU1

Linked Data

• dbSNP Id: rs1835810877

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16702446_16702454dup , CM000672.2:g.16702446_16702454dup	GRCh38
NC_000010.10:g.16744445_16744453dup , CM000672.1:g.16744445_16744453dup	GRCh37
NC_000010.9:g.16784451_16784459dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345264.10:c.599-7297_599-7289dup MANE Select	ENSP00000339521.5:n.599-7297_599-7289dup
ENST00000345264.9:c.599-7297_599-7289dup	ENSP00000339521.5:n.599-7297_599-7289dup
ENST00000377911.1:n.639-7297_639-7289dup
ENST00000377921.7:c.599-7297_599-7289dup	ENSP00000367154.3:n.599-7297_599-7289dup
ENST00000464074.6:n.665-7297_665-7289dup
ENST00000602389.1:c.440-7297_440-7289dup	ENSP00000473588.1:n.440-7297_440-7289dup
NM_012425.3:c.599-7297_599-7289dup	NP_036557.1:n.599-7297_599-7289dup
NM_152724.2:c.440-7297_440-7289dup	NP_689937.2:n.440-7297_440-7289dup
XM_005252552.2:c.598+50087_598+50095dup	XP_005252609.1:n.598+50087_598+50095dup
XM_011519613.1:c.449-7297_449-7289dup	XP_011517915.1:n.449-7297_449-7289dup
XM_005252552.4:c.598+50087_598+50095dup	XP_005252609.1:n.598+50087_598+50095dup
NM_012425.4:c.599-7297_599-7289dup MANE Select	NP_036557.1:n.599-7297_599-7289dup
NM_152724.3:c.440-7297_440-7289dup	NP_689937.2:n.440-7297_440-7289dup