Canonical Allele Identifier: CA137941721
Gene: CD2AP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.47576523delinsCT , CM000668.2:g.47576523delinsCT GRCh38
NC_000006.11:g.47544259delinsCT , CM000668.1:g.47544259delinsCT GRCh37
NC_000006.10:g.47652218delinsCT NCBI36
NG_008878.1:g.103735delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000359314.5:c.730-1delinsCT MANE Select ENSP00000352264.5:n.730-1delinsCT
ENST00000463175.1:n.11delinsCT
NM_012120.2:c.730-1delinsCT NP_036252.1:n.730-1delinsCT
XM_005248976.1:c.730-1delinsCT XP_005249033.1:n.730-1delinsCT
XM_005248977.2:c.730-1delinsCT XP_005249034.1:n.730-1delinsCT
XM_011514449.1:c.583-1delinsCT XP_011512751.1:n.583-1delinsCT
XM_011514449.2:c.583-1delinsCT XP_011512751.1:n.583-1delinsCT
XM_017010641.1:c.730-1delinsCT XP_016866130.1:n.730-1delinsCT
NM_012120.3:c.730-1delinsCT MANE Select NP_036252.1:n.730-1delinsCT
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