Canonical Allele Identifier: CA2259421256
Gene: CASC3 HGNC NCBI

Linked Data

dbSNP Id: rs1598423869

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40151915G>A , CM000679.2:g.40151915G>A GRCh38
NC_000017.10:g.38308168G>A , CM000679.1:g.38308168G>A GRCh37
NC_000017.9:g.35561694G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264645.12:c.298-9838G>A MANE Select ENSP00000264645.6:n.298-9838G>A
ENST00000264645.11:c.298-9838G>A ENSP00000264645.6:n.298-9838G>A
ENST00000418132.7:n.529-9838G>A
ENST00000581849.1:n.310-9838G>A
ENST00000584997.1:c.88-9838G>A ENSP00000467654.1:n.88-9838G>A
NM_007359.4:c.298-9838G>A NP_031385.2:n.298-9838G>A
XM_005257163.1:c.298-9838G>A XP_005257220.1:n.298-9838G>A
XR_934422.1:n.371-9838G>A
XM_005257163.2:c.298-9838G>A XP_005257220.1:n.298-9838G>A
XR_001752451.2:n.341-9838G>A
XR_002957984.1:n.341-9838G>A
XR_002957985.1:n.341-9838G>A
XR_934422.3:n.341-9838G>A
NM_007359.5:c.298-9838G>A MANE Select NP_031385.2:n.298-9838G>A