Canonical Allele Identifier: CA2777138216
Gene: MCM7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100098762_100098763insGGAAGTGCAGGAGGGAGGTGGAACTAGAATTT , CM000669.2:g.100098762_100098763insGGAAGTGCAGGAGGGAGGTGGAACTAGAATTT GRCh38
NC_000007.13:g.99696385_99696386insGGAAGTGCAGGAGGGAGGTGGAACTAGAATTT , CM000669.1:g.99696385_99696386insGGAAGTGCAGGAGGGAGGTGGAACTAGAATTT GRCh37
NC_000007.12:g.99534321_99534322insGGAAGTGCAGGAGGGAGGTGGAACTAGAATTT NCBI36
NG_016312.1:g.2256_2257insGGAAGTGCAGGAGGGAGGTGGAACTAGAATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000425308.6:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000411295.2:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000485286.6:n.1195-48_1195-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
ENST00000489841.6:n.1304-48_1304-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
ENST00000710813.1:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000518500.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000710814.1:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000518501.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000710815.1:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000518502.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000303887.10:c.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC MANE Select ENSP00000307288.5:n.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000303887.9:c.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000307288.5:n.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000343023.10:c.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000344006.6:n.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000354230.7:c.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000346171.3:n.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCA...
ENST00000425308.5:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000411295.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTG...
ENST00000463722.5:n.958-48_958-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
ENST00000485286.5:n.1172-48_1172-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
ENST00000489841.5:n.734-48_734-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
ENST00000491245.6:c.85+890_85+891insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
ENST00000621318.4:c.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC ENSP00000483795.1:n.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCA...
NM_001278595.1:c.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC NP_001265524.1:n.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTT...
NM_005916.4:c.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC NP_005907.3:n.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTC...
NM_182776.2:c.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC NP_877577.1:n.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC
XM_005250348.2:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC XP_005250405.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCAC...
XM_005250348.3:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC XP_005250405.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCAC...
XM_017012217.2:c.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC XP_016867706.1:n.262-48_262-47insAAATTCTAGTTCCACCTCCCTCCTGCAC...
NM_001278595.2:c.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC NP_001265524.1:n.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTT...
NM_005916.5:c.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC MANE Select NP_005907.3:n.583-48_583-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTC...
NM_182776.3:c.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC NP_877577.1:n.55-48_55-47insAAATTCTAGTTCCACCTCCCTCCTGCACTTCC