Canonical Allele Identifier: CA2684013521

Gene: MCM7

Linked Data

• gnomAD v4: 7-100098490-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098490C>A , CM000669.2:g.100098490C>A	GRCh38
NC_000007.13:g.99696113C>A , CM000669.1:g.99696113C>A	GRCh37
NC_000007.12:g.99534049C>A	NCBI36
NG_016312.1:g.1984C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.399+88G>T	ENSP00000411295.2:n.399+88G>T
ENST00000485286.6:n.1332+88G>T
ENST00000489841.6:n.1441+88G>T
ENST00000710813.1:c.399+88G>T	ENSP00000518500.1:n.399+88G>T
ENST00000710814.1:c.399+88G>T	ENSP00000518501.1:n.399+88G>T
ENST00000710815.1:c.399+88G>T	ENSP00000518502.1:n.399+88G>T
ENST00000303887.10:c.720+88G>T MANE Select	ENSP00000307288.5:n.720+88G>T
ENST00000303887.9:c.720+88G>T	ENSP00000307288.5:n.720+88G>T
ENST00000343023.10:c.720+88G>T	ENSP00000344006.6:n.720+88G>T
ENST00000354230.7:c.192+88G>T	ENSP00000346171.3:n.192+88G>T
ENST00000425308.5:c.399+88G>T	ENSP00000411295.1:n.399+88G>T
ENST00000463722.5:n.1095+88G>T
ENST00000485286.5:n.1309+88G>T
ENST00000489841.5:n.871+88G>T
ENST00000491245.6:c.85+1163G>T
ENST00000621318.4:c.192+88G>T	ENSP00000483795.1:n.192+88G>T
NM_001278595.1:c.192+88G>T	NP_001265524.1:n.192+88G>T
NM_005916.4:c.720+88G>T	NP_005907.3:n.720+88G>T
NM_182776.2:c.192+88G>T	NP_877577.1:n.192+88G>T
XM_005250348.2:c.399+88G>T	XP_005250405.1:n.399+88G>T
XM_005250348.3:c.399+88G>T	XP_005250405.1:n.399+88G>T
XM_017012217.2:c.399+88G>T	XP_016867706.1:n.399+88G>T
NM_001278595.2:c.192+88G>T	NP_001265524.1:n.192+88G>T
NM_005916.5:c.720+88G>T MANE Select	NP_005907.3:n.720+88G>T
NM_182776.3:c.192+88G>T	NP_877577.1:n.192+88G>T