Canonical Allele Identifier: CA1729340774

Gene: MCM7

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.275C=	ENSP00000411295.2:p.Thr92=
ENST00000485286.6:n.1208C=
ENST00000489841.6:n.1317C=
ENST00000710813.1:c.275C=	ENSP00000518500.1:p.Thr92=
ENST00000710814.1:c.275C=	ENSP00000518501.1:p.Thr92=
ENST00000710815.1:c.275C=	ENSP00000518502.1:p.Thr92=
ENST00000303887.10:c.596C= MANE Select	ENSP00000307288.5:p.Thr199=
ENST00000303887.9:c.596C=	ENSP00000307288.5:p.Thr199=
ENST00000343023.10:c.596C=	ENSP00000344006.6:p.Thr199=
ENST00000354230.7:c.68C=	ENSP00000346171.3:p.Thr23=
ENST00000425308.5:c.275C=	ENSP00000411295.1:p.Thr92=
ENST00000463722.5:n.971C=
ENST00000485286.5:n.1185C=
ENST00000489841.5:n.747C=
ENST00000491245.6:c.85+951C=
ENST00000621318.4:c.68C=	ENSP00000483795.1:p.Thr23=
NM_001278595.1:c.68C=	NP_001265524.1:p.Thr23=
NM_005916.4:c.596C=	NP_005907.3:p.Thr199=
NM_182776.2:c.68C=	NP_877577.1:p.Thr23=
XM_005250348.2:c.275C=	XP_005250405.1:p.Thr92=
XM_005250348.3:c.275C=	XP_005250405.1:p.Thr92=
XM_017012217.2:c.275C=	XP_016867706.1:p.Thr92=
NM_001278595.2:c.68C=	NP_001265524.1:p.Thr23=
NM_005916.5:c.596C= MANE Select	NP_005907.3:p.Thr199=
NM_182776.3:c.68C=	NP_877577.1:p.Thr23=