Canonical Allele Identifier: CA368451347

Gene: MCM7

Linked Data

• MyVariant Identifiers: chr7:g.99696222C>G (hg19) ; chr7:g.100098599C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098599C>G , CM000669.2:g.100098599C>G	GRCh38
NC_000007.13:g.99696222C>G , CM000669.1:g.99696222C>G	GRCh37
NC_000007.12:g.99534158C>G	NCBI36
NG_016312.1:g.2093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.378G>C	ENSP00000411295.2:p.Gln126His
ENST00000485286.6:n.1311G>C
ENST00000489841.6:n.1420G>C
ENST00000710813.1:c.378G>C	ENSP00000518500.1:p.Gln126His
ENST00000710814.1:c.378G>C	ENSP00000518501.1:p.Gln126His
ENST00000710815.1:c.378G>C	ENSP00000518502.1:p.Gln126His
ENST00000303887.10:c.699G>C MANE Select	ENSP00000307288.5:p.Gln233His
ENST00000303887.9:c.699G>C	ENSP00000307288.5:p.Gln233His
ENST00000343023.10:c.699G>C	ENSP00000344006.6:p.Gln233His
ENST00000354230.7:c.171G>C	ENSP00000346171.3:p.Gln57His
ENST00000425308.5:c.378G>C	ENSP00000411295.1:p.Gln126His
ENST00000463722.5:n.1074G>C
ENST00000485286.5:n.1288G>C
ENST00000489841.5:n.850G>C
ENST00000491245.6:c.85+1054G>C
ENST00000621318.4:c.171G>C	ENSP00000483795.1:p.Gln57His
NM_001278595.1:c.171G>C	NP_001265524.1:p.Gln57His
NM_005916.4:c.699G>C	NP_005907.3:p.Gln233His
NM_182776.2:c.171G>C	NP_877577.1:p.Gln57His
XM_005250348.2:c.378G>C	XP_005250405.1:p.Gln126His
XM_005250348.3:c.378G>C	XP_005250405.1:p.Gln126His
XM_017012217.2:c.378G>C	XP_016867706.1:p.Gln126His
NM_001278595.2:c.171G>C	NP_001265524.1:p.Gln57His
NM_005916.5:c.699G>C MANE Select	NP_005907.3:p.Gln233His
NM_182776.3:c.171G>C	NP_877577.1:p.Gln57His