Canonical Allele Identifier: CA1893248063
Gene: RSU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16702430C= , CM000672.2:g.16702430C= GRCh38
NC_000010.10:g.16744429C= , CM000672.1:g.16744429C= GRCh37
NC_000010.9:g.16784435C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000345264.10:c.599-7275G= MANE Select ENSP00000339521.5:n.599-7275G=
ENST00000345264.9:c.599-7275G= ENSP00000339521.5:n.599-7275G=
ENST00000377911.1:n.639-7275G=
ENST00000377921.7:c.599-7275G= ENSP00000367154.3:n.599-7275G=
ENST00000464074.6:n.665-7275G=
ENST00000602389.1:c.440-7275G= ENSP00000473588.1:n.440-7275G=
NM_012425.3:c.599-7275G= NP_036557.1:n.599-7275G=
NM_152724.2:c.440-7275G= NP_689937.2:n.440-7275G=
XM_005252552.2:c.598+50109G= XP_005252609.1:n.598+50109G=
XM_011519613.1:c.449-7275G= XP_011517915.1:n.449-7275G=
XM_005252552.4:c.598+50109G= XP_005252609.1:n.598+50109G=
NM_012425.4:c.599-7275G= MANE Select NP_036557.1:n.599-7275G=
NM_152724.3:c.440-7275G= NP_689937.2:n.440-7275G=