Canonical Allele Identifier: CA4374232

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100099728A>G , CM000669.2:g.100099728A>G	GRCh38
NC_000007.13:g.99697351A>G , CM000669.1:g.99697351A>G	GRCh37
NC_000007.12:g.99535287A>G	NCBI36
NG_016312.1:g.3222A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.-185T>C	ENSP00000411295.2:n.-185T>C
ENST00000485286.6:n.674T>C
ENST00000489841.6:n.783T>C
ENST00000710813.1:c.-185T>C	ENSP00000518500.1:n.-185T>C
ENST00000710814.1:c.-185T>C	ENSP00000518501.1:n.-185T>C
ENST00000710815.1:c.-185T>C	ENSP00000518502.1:n.-185T>C
ENST00000303887.10:c.137T>C MANE Select	ENSP00000307288.5:p.Val46Ala
ENST00000303887.9:c.137T>C	ENSP00000307288.5:p.Val46Ala
ENST00000343023.10:c.137T>C	ENSP00000344006.6:p.Val46Ala
ENST00000354230.7:c.-467T>C	ENSP00000346171.3:n.-467T>C
ENST00000425308.5:c.-185T>C	ENSP00000411295.1:n.-185T>C
ENST00000463722.5:n.252T>C
ENST00000465688.1:n.217T>C
ENST00000465738.1:n.406T>C
ENST00000467516.5:n.367T>C
ENST00000485286.5:n.651T>C
ENST00000489841.5:n.213T>C
ENST00000491245.6:c.10T>C
ENST00000621318.4:c.-467T>C	ENSP00000483795.1:n.-467T>C
NM_001278595.1:c.-467T>C	NP_001265524.1:n.-467T>C
NM_005916.4:c.137T>C	NP_005907.3:p.Val46Ala
NM_182776.2:c.-467T>C	NP_877577.1:n.-467T>C
XM_005250348.2:c.-185T>C	XP_005250405.1:n.-185T>C
XM_005250348.3:c.-185T>C	XP_005250405.1:n.-185T>C
XM_017012217.2:c.-185T>C	XP_016867706.1:n.-185T>C
NM_001278595.2:c.-467T>C	NP_001265524.1:n.-467T>C
NM_005916.5:c.137T>C MANE Select	NP_005907.3:p.Val46Ala
NM_182776.3:c.-467T>C	NP_877577.1:n.-467T>C