Canonical Allele Identifier: CA1729340938

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098853_100098857delinsCAACA , CM000669.2:g.100098853_100098857delinsCAACA	GRCh38
NC_000007.13:g.99696476_99696480delinsCAACA , CM000669.1:g.99696476_99696480delinsCAACA	GRCh37
NC_000007.12:g.99534412_99534416delinsCAACA	NCBI36
NG_016312.1:g.2347_2351delinsCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.262-142_262-138delinsTGTTG	ENSP00000411295.2:n.262-142_262-138delinsTGTTG
ENST00000485286.6:n.1195-142_1195-138delinsTGTTG
ENST00000489841.6:n.1304-142_1304-138delinsTGTTG
ENST00000710813.1:c.262-142_262-138delinsTGTTG	ENSP00000518500.1:n.262-142_262-138delinsTGTTG
ENST00000710814.1:c.262-142_262-138delinsTGTTG	ENSP00000518501.1:n.262-142_262-138delinsTGTTG
ENST00000710815.1:c.262-142_262-138delinsTGTTG	ENSP00000518502.1:n.262-142_262-138delinsTGTTG
ENST00000303887.10:c.583-142_583-138delinsTGTTG MANE Select	ENSP00000307288.5:n.583-142_583-138delinsTGTTG
ENST00000303887.9:c.583-142_583-138delinsTGTTG	ENSP00000307288.5:n.583-142_583-138delinsTGTTG
ENST00000343023.10:c.583-142_583-138delinsTGTTG	ENSP00000344006.6:n.583-142_583-138delinsTGTTG
ENST00000354230.7:c.55-142_55-138delinsTGTTG	ENSP00000346171.3:n.55-142_55-138delinsTGTTG
ENST00000425308.5:c.262-142_262-138delinsTGTTG	ENSP00000411295.1:n.262-142_262-138delinsTGTTG
ENST00000463722.5:n.958-142_958-138delinsTGTTG
ENST00000485286.5:n.1172-142_1172-138delinsTGTTG
ENST00000489841.5:n.734-142_734-138delinsTGTTG
ENST00000491245.6:c.85+796_85+800delinsTGTTG
ENST00000621318.4:c.55-142_55-138delinsTGTTG	ENSP00000483795.1:n.55-142_55-138delinsTGTTG
NM_001278595.1:c.55-142_55-138delinsTGTTG	NP_001265524.1:n.55-142_55-138delinsTGTTG
NM_005916.4:c.583-142_583-138delinsTGTTG	NP_005907.3:n.583-142_583-138delinsTGTTG
NM_182776.2:c.55-142_55-138delinsTGTTG	NP_877577.1:n.55-142_55-138delinsTGTTG
XM_005250348.2:c.262-142_262-138delinsTGTTG	XP_005250405.1:n.262-142_262-138delinsTGTTG
XM_005250348.3:c.262-142_262-138delinsTGTTG	XP_005250405.1:n.262-142_262-138delinsTGTTG
XM_017012217.2:c.262-142_262-138delinsTGTTG	XP_016867706.1:n.262-142_262-138delinsTGTTG
NM_001278595.2:c.55-142_55-138delinsTGTTG	NP_001265524.1:n.55-142_55-138delinsTGTTG
NM_005916.5:c.583-142_583-138delinsTGTTG MANE Select	NP_005907.3:n.583-142_583-138delinsTGTTG
NM_182776.3:c.55-142_55-138delinsTGTTG	NP_877577.1:n.55-142_55-138delinsTGTTG