Canonical Allele Identifier: CA1729340813

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098747C= , CM000669.2:g.100098747C=	GRCh38
NC_000007.13:g.99696370C= , CM000669.1:g.99696370C=	GRCh37
NC_000007.12:g.99534306C=	NCBI36
NG_016312.1:g.2241C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000425308.6:c.262-32G=	ENSP00000411295.2:n.262-32G=
ENST00000485286.6:n.1195-32G=
ENST00000489841.6:n.1304-32G=
ENST00000710813.1:c.262-32G=	ENSP00000518500.1:n.262-32G=
ENST00000710814.1:c.262-32G=	ENSP00000518501.1:n.262-32G=
ENST00000710815.1:c.262-32G=	ENSP00000518502.1:n.262-32G=
ENST00000303887.10:c.583-32G= MANE Select	ENSP00000307288.5:n.583-32G=
ENST00000303887.9:c.583-32G=	ENSP00000307288.5:n.583-32G=
ENST00000343023.10:c.583-32G=	ENSP00000344006.6:n.583-32G=
ENST00000354230.7:c.55-32G=	ENSP00000346171.3:n.55-32G=
ENST00000425308.5:c.262-32G=	ENSP00000411295.1:n.262-32G=
ENST00000463722.5:n.958-32G=
ENST00000485286.5:n.1172-32G=
ENST00000489841.5:n.734-32G=
ENST00000491245.6:c.85+906G=
ENST00000621318.4:c.55-32G=	ENSP00000483795.1:n.55-32G=
NM_001278595.1:c.55-32G=	NP_001265524.1:n.55-32G=
NM_005916.4:c.583-32G=	NP_005907.3:n.583-32G=
NM_182776.2:c.55-32G=	NP_877577.1:n.55-32G=
XM_005250348.2:c.262-32G=	XP_005250405.1:n.262-32G=
XM_005250348.3:c.262-32G=	XP_005250405.1:n.262-32G=
XM_017012217.2:c.262-32G=	XP_016867706.1:n.262-32G=
NM_001278595.2:c.55-32G=	NP_001265524.1:n.55-32G=
NM_005916.5:c.583-32G= MANE Select	NP_005907.3:n.583-32G=
NM_182776.3:c.55-32G=	NP_877577.1:n.55-32G=