Canonical Allele Identifier: CA2259419150
Gene: CASC3 HGNC NCBI

Linked Data

dbSNP Id: rs1988886013
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40147306A>G , CM000679.2:g.40147306A>G GRCh38
NC_000017.10:g.38303559A>G , CM000679.1:g.38303559A>G GRCh37
NC_000017.9:g.35557085A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264645.12:c.297+5699A>G MANE Select ENSP00000264645.6:n.297+5699A>G
ENST00000264645.11:c.297+5699A>G ENSP00000264645.6:n.297+5699A>G
ENST00000418132.7:n.528+5699A>G
ENST00000581849.1:n.309+5699A>G
ENST00000584997.1:c.87+5699A>G ENSP00000467654.1:n.87+5699A>G
NM_007359.4:c.297+5699A>G NP_031385.2:n.297+5699A>G
XM_005257163.1:c.297+5699A>G XP_005257220.1:n.297+5699A>G
XR_934422.1:n.370+5699A>G
XM_005257163.2:c.297+5699A>G XP_005257220.1:n.297+5699A>G
XR_001752451.2:n.340+5699A>G
XR_002957984.1:n.340+5699A>G
XR_002957985.1:n.340+5699A>G
XR_934422.3:n.340+5699A>G
NM_007359.5:c.297+5699A>G MANE Select NP_031385.2:n.297+5699A>G
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