Canonical Allele Identifier: CA1893248050

Gene: RSU1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16702422_16702424delinsCAA , CM000672.2:g.16702422_16702424delinsCAA	GRCh38
NC_000010.10:g.16744421_16744423delinsCAA , CM000672.1:g.16744421_16744423delinsCAA	GRCh37
NC_000010.9:g.16784427_16784429delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345264.10:c.599-7269_599-7267delinsTTG MANE Select	ENSP00000339521.5:n.599-7269_599-7267delinsTTG
ENST00000345264.9:c.599-7269_599-7267delinsTTG	ENSP00000339521.5:n.599-7269_599-7267delinsTTG
ENST00000377911.1:n.639-7269_639-7267delinsTTG
ENST00000377921.7:c.599-7269_599-7267delinsTTG	ENSP00000367154.3:n.599-7269_599-7267delinsTTG
ENST00000464074.6:n.665-7269_665-7267delinsTTG
ENST00000602389.1:c.440-7269_440-7267delinsTTG	ENSP00000473588.1:n.440-7269_440-7267delinsTTG
NM_012425.3:c.599-7269_599-7267delinsTTG	NP_036557.1:n.599-7269_599-7267delinsTTG
NM_152724.2:c.440-7269_440-7267delinsTTG	NP_689937.2:n.440-7269_440-7267delinsTTG
XM_005252552.2:c.598+50115_598+50117delinsTTG	XP_005252609.1:n.598+50115_598+50117delinsTTG
XM_011519613.1:c.449-7269_449-7267delinsTTG	XP_011517915.1:n.449-7269_449-7267delinsTTG
XM_005252552.4:c.598+50115_598+50117delinsTTG	XP_005252609.1:n.598+50115_598+50117delinsTTG
NM_012425.4:c.599-7269_599-7267delinsTTG MANE Select	NP_036557.1:n.599-7269_599-7267delinsTTG
NM_152724.3:c.440-7269_440-7267delinsTTG	NP_689937.2:n.440-7269_440-7267delinsTTG