Canonical Allele Identifier: CA1729340513

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098432T= , CM000669.2:g.100098432T=	GRCh38
NC_000007.13:g.99696055T= , CM000669.1:g.99696055T=	GRCh37
NC_000007.12:g.99533991T=	NCBI36
NG_016312.1:g.1926T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.400-142A=	ENSP00000411295.2:n.400-142A=
ENST00000485286.6:n.1333-142A=
ENST00000489841.6:n.1442-142A=
ENST00000710813.1:c.400-142A=	ENSP00000518500.1:n.400-142A=
ENST00000710814.1:c.400-142A=	ENSP00000518501.1:n.400-142A=
ENST00000710815.1:c.400-142A=	ENSP00000518502.1:n.400-142A=
ENST00000303887.10:c.721-142A= MANE Select	ENSP00000307288.5:n.721-142A=
ENST00000303887.9:c.721-142A=	ENSP00000307288.5:n.721-142A=
ENST00000343023.10:c.721-142A=	ENSP00000344006.6:n.721-142A=
ENST00000354230.7:c.193-142A=	ENSP00000346171.3:n.193-142A=
ENST00000425308.5:c.400-142A=	ENSP00000411295.1:n.400-142A=
ENST00000463722.5:n.1096-142A=
ENST00000485286.5:n.1310-142A=
ENST00000489841.5:n.872-142A=
ENST00000491245.6:c.85+1221A=
ENST00000621318.4:c.193-142A=	ENSP00000483795.1:n.193-142A=
NM_001278595.1:c.193-142A=	NP_001265524.1:n.193-142A=
NM_005916.4:c.721-142A=	NP_005907.3:n.721-142A=
NM_182776.2:c.193-142A=	NP_877577.1:n.193-142A=
XM_005250348.2:c.400-142A=	XP_005250405.1:n.400-142A=
XM_005250348.3:c.400-142A=	XP_005250405.1:n.400-142A=
XM_017012217.2:c.400-142A=	XP_016867706.1:n.400-142A=
NM_001278595.2:c.193-142A=	NP_001265524.1:n.193-142A=
NM_005916.5:c.721-142A= MANE Select	NP_005907.3:n.721-142A=
NM_182776.3:c.193-142A=	NP_877577.1:n.193-142A=