Canonical Allele Identifier: CA1893248136

Gene: RSU1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16702522_16702523delinsAC , CM000672.2:g.16702522_16702523delinsAC	GRCh38
NC_000010.10:g.16744521_16744522delinsAC , CM000672.1:g.16744521_16744522delinsAC	GRCh37
NC_000010.9:g.16784527_16784528delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345264.10:c.599-7368_599-7367delinsGT MANE Select	ENSP00000339521.5:n.599-7368_599-7367delinsGT
ENST00000345264.9:c.599-7368_599-7367delinsGT	ENSP00000339521.5:n.599-7368_599-7367delinsGT
ENST00000377911.1:n.639-7368_639-7367delinsGT
ENST00000377921.7:c.599-7368_599-7367delinsGT	ENSP00000367154.3:n.599-7368_599-7367delinsGT
ENST00000464074.6:n.665-7368_665-7367delinsGT
ENST00000602389.1:c.440-7368_440-7367delinsGT	ENSP00000473588.1:n.440-7368_440-7367delinsGT
NM_012425.3:c.599-7368_599-7367delinsGT	NP_036557.1:n.599-7368_599-7367delinsGT
NM_152724.2:c.440-7368_440-7367delinsGT	NP_689937.2:n.440-7368_440-7367delinsGT
XM_005252552.2:c.598+50016_598+50017delinsGT	XP_005252609.1:n.598+50016_598+50017delinsGT
XM_011519613.1:c.449-7368_449-7367delinsGT	XP_011517915.1:n.449-7368_449-7367delinsGT
XM_005252552.4:c.598+50016_598+50017delinsGT	XP_005252609.1:n.598+50016_598+50017delinsGT
NM_012425.4:c.599-7368_599-7367delinsGT MANE Select	NP_036557.1:n.599-7368_599-7367delinsGT
NM_152724.3:c.440-7368_440-7367delinsGT	NP_689937.2:n.440-7368_440-7367delinsGT