Canonical Allele Identifier: CA4373983

Gene: MCM7

Linked Data

• dbSNP Id: rs138501873
• ExAC: 7:99696325 G / A
• gnomAD v2: 7-99696325-G-A
• gnomAD v3: 7-100098702-G-A
• gnomAD v4: 7-100098702-G-A
• MyVariant Identifiers: chr7:g.99696325G>A (hg19) ; chr7:g.100098702G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098702G>A , CM000669.2:g.100098702G>A	GRCh38
NC_000007.13:g.99696325G>A , CM000669.1:g.99696325G>A	GRCh37
NC_000007.12:g.99534261G>A	NCBI36
NG_016312.1:g.2196G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.275C>T	ENSP00000411295.2:p.Thr92Ile
ENST00000485286.6:n.1208C>T
ENST00000489841.6:n.1317C>T
ENST00000710813.1:c.275C>T	ENSP00000518500.1:p.Thr92Ile
ENST00000710814.1:c.275C>T	ENSP00000518501.1:p.Thr92Ile
ENST00000710815.1:c.275C>T	ENSP00000518502.1:p.Thr92Ile
ENST00000303887.10:c.596C>T MANE Select	ENSP00000307288.5:p.Thr199Ile
ENST00000303887.9:c.596C>T	ENSP00000307288.5:p.Thr199Ile
ENST00000343023.10:c.596C>T	ENSP00000344006.6:p.Thr199Ile
ENST00000354230.7:c.68C>T	ENSP00000346171.3:p.Thr23Ile
ENST00000425308.5:c.275C>T	ENSP00000411295.1:p.Thr92Ile
ENST00000463722.5:n.971C>T
ENST00000485286.5:n.1185C>T
ENST00000489841.5:n.747C>T
ENST00000491245.6:c.85+951C>T
ENST00000621318.4:c.68C>T	ENSP00000483795.1:p.Thr23Ile
NM_001278595.1:c.68C>T	NP_001265524.1:p.Thr23Ile
NM_005916.4:c.596C>T	NP_005907.3:p.Thr199Ile
NM_182776.2:c.68C>T	NP_877577.1:p.Thr23Ile
XM_005250348.2:c.275C>T	XP_005250405.1:p.Thr92Ile
XM_005250348.3:c.275C>T	XP_005250405.1:p.Thr92Ile
XM_017012217.2:c.275C>T	XP_016867706.1:p.Thr92Ile
NM_001278595.2:c.68C>T	NP_001265524.1:p.Thr23Ile
NM_005916.5:c.596C>T MANE Select	NP_005907.3:p.Thr199Ile
NM_182776.3:c.68C>T	NP_877577.1:p.Thr23Ile