Canonical Allele Identifier: CA368452130

Gene: MCM7

Linked Data

• MyVariant Identifiers: chr7:g.99696304C>G (hg19) ; chr7:g.100098681C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098681C>G , CM000669.2:g.100098681C>G	GRCh38
NC_000007.13:g.99696304C>G , CM000669.1:g.99696304C>G	GRCh37
NC_000007.12:g.99534240C>G	NCBI36
NG_016312.1:g.2175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.296G>C	ENSP00000411295.2:p.Cys99Ser
ENST00000485286.6:n.1229G>C
ENST00000489841.6:n.1338G>C
ENST00000710813.1:c.296G>C	ENSP00000518500.1:p.Cys99Ser
ENST00000710814.1:c.296G>C	ENSP00000518501.1:p.Cys99Ser
ENST00000710815.1:c.296G>C	ENSP00000518502.1:p.Cys99Ser
ENST00000303887.10:c.617G>C MANE Select	ENSP00000307288.5:p.Cys206Ser
ENST00000303887.9:c.617G>C	ENSP00000307288.5:p.Cys206Ser
ENST00000343023.10:c.617G>C	ENSP00000344006.6:p.Cys206Ser
ENST00000354230.7:c.89G>C	ENSP00000346171.3:p.Cys30Ser
ENST00000425308.5:c.296G>C	ENSP00000411295.1:p.Cys99Ser
ENST00000463722.5:n.992G>C
ENST00000485286.5:n.1206G>C
ENST00000489841.5:n.768G>C
ENST00000491245.6:c.85+972G>C
ENST00000621318.4:c.89G>C	ENSP00000483795.1:p.Cys30Ser
NM_001278595.1:c.89G>C	NP_001265524.1:p.Cys30Ser
NM_005916.4:c.617G>C	NP_005907.3:p.Cys206Ser
NM_182776.2:c.89G>C	NP_877577.1:p.Cys30Ser
XM_005250348.2:c.296G>C	XP_005250405.1:p.Cys99Ser
XM_005250348.3:c.296G>C	XP_005250405.1:p.Cys99Ser
XM_017012217.2:c.296G>C	XP_016867706.1:p.Cys99Ser
NM_001278595.2:c.89G>C	NP_001265524.1:p.Cys30Ser
NM_005916.5:c.617G>C MANE Select	NP_005907.3:p.Cys206Ser
NM_182776.3:c.89G>C	NP_877577.1:p.Cys30Ser