Canonical Allele Identifier: CA1729340888

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098815_100098816delinsGT , CM000669.2:g.100098815_100098816delinsGT	GRCh38
NC_000007.13:g.99696438_99696439delinsGT , CM000669.1:g.99696438_99696439delinsGT	GRCh37
NC_000007.12:g.99534374_99534375delinsGT	NCBI36
NG_016312.1:g.2309_2310delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.262-101_262-100delinsAC	ENSP00000411295.2:n.262-101_262-100delinsAC
ENST00000485286.6:n.1195-101_1195-100delinsAC
ENST00000489841.6:n.1304-101_1304-100delinsAC
ENST00000710813.1:c.262-101_262-100delinsAC	ENSP00000518500.1:n.262-101_262-100delinsAC
ENST00000710814.1:c.262-101_262-100delinsAC	ENSP00000518501.1:n.262-101_262-100delinsAC
ENST00000710815.1:c.262-101_262-100delinsAC	ENSP00000518502.1:n.262-101_262-100delinsAC
ENST00000303887.10:c.583-101_583-100delinsAC MANE Select	ENSP00000307288.5:n.583-101_583-100delinsAC
ENST00000303887.9:c.583-101_583-100delinsAC	ENSP00000307288.5:n.583-101_583-100delinsAC
ENST00000343023.10:c.583-101_583-100delinsAC	ENSP00000344006.6:n.583-101_583-100delinsAC
ENST00000354230.7:c.55-101_55-100delinsAC	ENSP00000346171.3:n.55-101_55-100delinsAC
ENST00000425308.5:c.262-101_262-100delinsAC	ENSP00000411295.1:n.262-101_262-100delinsAC
ENST00000463722.5:n.958-101_958-100delinsAC
ENST00000485286.5:n.1172-101_1172-100delinsAC
ENST00000489841.5:n.734-101_734-100delinsAC
ENST00000491245.6:c.85+837_85+838delinsAC
ENST00000621318.4:c.55-101_55-100delinsAC	ENSP00000483795.1:n.55-101_55-100delinsAC
NM_001278595.1:c.55-101_55-100delinsAC	NP_001265524.1:n.55-101_55-100delinsAC
NM_005916.4:c.583-101_583-100delinsAC	NP_005907.3:n.583-101_583-100delinsAC
NM_182776.2:c.55-101_55-100delinsAC	NP_877577.1:n.55-101_55-100delinsAC
XM_005250348.2:c.262-101_262-100delinsAC	XP_005250405.1:n.262-101_262-100delinsAC
XM_005250348.3:c.262-101_262-100delinsAC	XP_005250405.1:n.262-101_262-100delinsAC
XM_017012217.2:c.262-101_262-100delinsAC	XP_016867706.1:n.262-101_262-100delinsAC
NM_001278595.2:c.55-101_55-100delinsAC	NP_001265524.1:n.55-101_55-100delinsAC
NM_005916.5:c.583-101_583-100delinsAC MANE Select	NP_005907.3:n.583-101_583-100delinsAC
NM_182776.3:c.55-101_55-100delinsAC	NP_877577.1:n.55-101_55-100delinsAC