Canonical Allele Identifier: CA1729340447

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098342C= , CM000669.2:g.100098342C=	GRCh38
NC_000007.13:g.99695965C= , CM000669.1:g.99695965C=	GRCh37
NC_000007.12:g.99533901C=	NCBI36
NG_016312.1:g.1836C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.400-52G=	ENSP00000411295.2:n.400-52G=
ENST00000485286.6:n.1333-52G=
ENST00000489841.6:n.1442-52G=
ENST00000710813.1:c.400-52G=	ENSP00000518500.1:n.400-52G=
ENST00000710814.1:c.400-52G=	ENSP00000518501.1:n.400-52G=
ENST00000710815.1:c.400-52G=	ENSP00000518502.1:n.400-52G=
ENST00000303887.10:c.721-52G= MANE Select	ENSP00000307288.5:n.721-52G=
ENST00000303887.9:c.721-52G=	ENSP00000307288.5:n.721-52G=
ENST00000343023.10:c.721-52G=	ENSP00000344006.6:n.721-52G=
ENST00000354230.7:c.193-52G=	ENSP00000346171.3:n.193-52G=
ENST00000425308.5:c.400-52G=	ENSP00000411295.1:n.400-52G=
ENST00000463722.5:n.1096-52G=
ENST00000485286.5:n.1310-52G=
ENST00000489841.5:n.872-52G=
ENST00000491245.6:c.85+1311G=
ENST00000621318.4:c.193-52G=	ENSP00000483795.1:n.193-52G=
NM_001278595.1:c.193-52G=	NP_001265524.1:n.193-52G=
NM_005916.4:c.721-52G=	NP_005907.3:n.721-52G=
NM_182776.2:c.193-52G=	NP_877577.1:n.193-52G=
XM_005250348.2:c.400-52G=	XP_005250405.1:n.400-52G=
XM_005250348.3:c.400-52G=	XP_005250405.1:n.400-52G=
XM_017012217.2:c.400-52G=	XP_016867706.1:n.400-52G=
NM_001278595.2:c.193-52G=	NP_001265524.1:n.193-52G=
NM_005916.5:c.721-52G= MANE Select	NP_005907.3:n.721-52G=
NM_182776.3:c.193-52G=	NP_877577.1:n.193-52G=