Canonical Allele Identifier: CA2259421287
Community Standard Title: NM_007359.5(CASC3):c.298-9762C=
Gene: CASC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40151991C= , CM000679.2:g.40151991C= GRCh38
NC_000017.10:g.38308244C= , CM000679.1:g.38308244C= GRCh37
NC_000017.9:g.35561770C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_007359.5:c.298-9762C= MANE Select NP_031385.2:n.298-9762C=
ENST00000264645.12:c.298-9762C= MANE Select ENSP00000264645.6:n.298-9762C=
NM_007359.4:c.298-9762C= NP_031385.2:n.298-9762C=
ENST00000264645.11:c.298-9762C= ENSP00000264645.6:n.298-9762C=
ENST00000418132.7:n.529-9762C=
ENST00000581849.1:n.310-9762C=
ENST00000584997.1:c.88-9762C= ENSP00000467654.1:n.88-9762C=
XM_005257163.1:c.298-9762C= XP_005257220.1:n.298-9762C=
XM_005257163.2:c.298-9762C= XP_005257220.1:n.298-9762C=
XR_001752451.2:n.341-9762C=
XR_002957984.1:n.341-9762C=
XR_002957985.1:n.341-9762C=
XR_934422.1:n.371-9762C=
XR_934422.3:n.341-9762C=