Canonical Allele Identifier: CA1729340910

Gene: MCM7

Linked Data

• dbSNP Id: rs1795780879
• gnomAD v4: 7-100098833-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098833C>A , CM000669.2:g.100098833C>A	GRCh38
NC_000007.13:g.99696456C>A , CM000669.1:g.99696456C>A	GRCh37
NC_000007.12:g.99534392C>A	NCBI36
NG_016312.1:g.2327C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.262-118G>T	ENSP00000411295.2:n.262-118G>T
ENST00000485286.6:n.1195-118G>T
ENST00000489841.6:n.1304-118G>T
ENST00000710813.1:c.262-118G>T	ENSP00000518500.1:n.262-118G>T
ENST00000710814.1:c.262-118G>T	ENSP00000518501.1:n.262-118G>T
ENST00000710815.1:c.262-118G>T	ENSP00000518502.1:n.262-118G>T
ENST00000303887.10:c.583-118G>T MANE Select	ENSP00000307288.5:n.583-118G>T
ENST00000303887.9:c.583-118G>T	ENSP00000307288.5:n.583-118G>T
ENST00000343023.10:c.583-118G>T	ENSP00000344006.6:n.583-118G>T
ENST00000354230.7:c.55-118G>T	ENSP00000346171.3:n.55-118G>T
ENST00000425308.5:c.262-118G>T	ENSP00000411295.1:n.262-118G>T
ENST00000463722.5:n.958-118G>T
ENST00000485286.5:n.1172-118G>T
ENST00000489841.5:n.734-118G>T
ENST00000491245.6:c.85+820G>T
ENST00000621318.4:c.55-118G>T	ENSP00000483795.1:n.55-118G>T
NM_001278595.1:c.55-118G>T	NP_001265524.1:n.55-118G>T
NM_005916.4:c.583-118G>T	NP_005907.3:n.583-118G>T
NM_182776.2:c.55-118G>T	NP_877577.1:n.55-118G>T
XM_005250348.2:c.262-118G>T	XP_005250405.1:n.262-118G>T
XM_005250348.3:c.262-118G>T	XP_005250405.1:n.262-118G>T
XM_017012217.2:c.262-118G>T	XP_016867706.1:n.262-118G>T
NM_001278595.2:c.55-118G>T	NP_001265524.1:n.55-118G>T
NM_005916.5:c.583-118G>T MANE Select	NP_005907.3:n.583-118G>T
NM_182776.3:c.55-118G>T	NP_877577.1:n.55-118G>T