Canonical Allele Identifier: CA2684013753
Gene: MCM7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100098856_100098858del , CM000669.2:g.100098856_100098858del GRCh38
NC_000007.13:g.99696479_99696481del , CM000669.1:g.99696479_99696481del GRCh37
NC_000007.12:g.99534415_99534417del NCBI36
NG_016312.1:g.2350_2352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425308.6:c.262-137_262-135del ENSP00000411295.2:n.262-137_262-135del
ENST00000485286.6:n.1195-137_1195-135del
ENST00000489841.6:n.1304-137_1304-135del
ENST00000710813.1:c.262-137_262-135del ENSP00000518500.1:n.262-137_262-135del
ENST00000710814.1:c.262-137_262-135del ENSP00000518501.1:n.262-137_262-135del
ENST00000710815.1:c.262-137_262-135del ENSP00000518502.1:n.262-137_262-135del
ENST00000303887.10:c.583-137_583-135del MANE Select ENSP00000307288.5:n.583-137_583-135del
ENST00000303887.9:c.583-137_583-135del ENSP00000307288.5:n.583-137_583-135del
ENST00000343023.10:c.583-137_583-135del ENSP00000344006.6:n.583-137_583-135del
ENST00000354230.7:c.55-137_55-135del ENSP00000346171.3:n.55-137_55-135del
ENST00000425308.5:c.262-137_262-135del ENSP00000411295.1:n.262-137_262-135del
ENST00000463722.5:n.958-137_958-135del
ENST00000485286.5:n.1172-137_1172-135del
ENST00000489841.5:n.734-137_734-135del
ENST00000491245.6:c.85+801_85+803del
ENST00000621318.4:c.55-137_55-135del ENSP00000483795.1:n.55-137_55-135del
NM_001278595.1:c.55-137_55-135del NP_001265524.1:n.55-137_55-135del
NM_005916.4:c.583-137_583-135del NP_005907.3:n.583-137_583-135del
NM_182776.2:c.55-137_55-135del NP_877577.1:n.55-137_55-135del
XM_005250348.2:c.262-137_262-135del XP_005250405.1:n.262-137_262-135del
XM_005250348.3:c.262-137_262-135del XP_005250405.1:n.262-137_262-135del
XM_017012217.2:c.262-137_262-135del XP_016867706.1:n.262-137_262-135del
NM_001278595.2:c.55-137_55-135del NP_001265524.1:n.55-137_55-135del
NM_005916.5:c.583-137_583-135del MANE Select NP_005907.3:n.583-137_583-135del
NM_182776.3:c.55-137_55-135del NP_877577.1:n.55-137_55-135del