Canonical Allele Identifier: CA368451999

Gene: MCM7

Linked Data

• MyVariant Identifiers: chr7:g.99696293C>T (hg19) ; chr7:g.100098670C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098670C>T , CM000669.2:g.100098670C>T	GRCh38
NC_000007.13:g.99696293C>T , CM000669.1:g.99696293C>T	GRCh37
NC_000007.12:g.99534229C>T	NCBI36
NG_016312.1:g.2164C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.307G>A	ENSP00000411295.2:p.Glu103Lys
ENST00000485286.6:n.1240G>A
ENST00000489841.6:n.1349G>A
ENST00000710813.1:c.307G>A	ENSP00000518500.1:p.Glu103Lys
ENST00000710814.1:c.307G>A	ENSP00000518501.1:p.Glu103Lys
ENST00000710815.1:c.307G>A	ENSP00000518502.1:p.Glu103Lys
ENST00000303887.10:c.628G>A MANE Select	ENSP00000307288.5:p.Glu210Lys
ENST00000303887.9:c.628G>A	ENSP00000307288.5:p.Glu210Lys
ENST00000343023.10:c.628G>A	ENSP00000344006.6:p.Glu210Lys
ENST00000354230.7:c.100G>A	ENSP00000346171.3:p.Glu34Lys
ENST00000425308.5:c.307G>A	ENSP00000411295.1:p.Glu103Lys
ENST00000463722.5:n.1003G>A
ENST00000485286.5:n.1217G>A
ENST00000489841.5:n.779G>A
ENST00000491245.6:c.85+983G>A
ENST00000621318.4:c.100G>A	ENSP00000483795.1:p.Glu34Lys
NM_001278595.1:c.100G>A	NP_001265524.1:p.Glu34Lys
NM_005916.4:c.628G>A	NP_005907.3:p.Glu210Lys
NM_182776.2:c.100G>A	NP_877577.1:p.Glu34Lys
XM_005250348.2:c.307G>A	XP_005250405.1:p.Glu103Lys
XM_005250348.3:c.307G>A	XP_005250405.1:p.Glu103Lys
XM_017012217.2:c.307G>A	XP_016867706.1:p.Glu103Lys
NM_001278595.2:c.100G>A	NP_001265524.1:p.Glu34Lys
NM_005916.5:c.628G>A MANE Select	NP_005907.3:p.Glu210Lys
NM_182776.3:c.100G>A	NP_877577.1:p.Glu34Lys