Canonical Allele Identifier: CA456703915

Gene: MCM7

Linked Data

• dbSNP Id: rs1175667881
• gnomAD v3: 7-100098674-G-A
• gnomAD v4: 7-100098674-G-A
• MyVariant Identifiers: chr7:g.99696297G>A (hg19) ; chr7:g.100098674G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098674G>A , CM000669.2:g.100098674G>A	GRCh38
NC_000007.13:g.99696297G>A , CM000669.1:g.99696297G>A	GRCh37
NC_000007.12:g.99534233G>A	NCBI36
NG_016312.1:g.2168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.303C>T	ENSP00000411295.2:p.Ser101=
ENST00000485286.6:n.1236C>T
ENST00000489841.6:n.1345C>T
ENST00000710813.1:c.303C>T	ENSP00000518500.1:p.Ser101=
ENST00000710814.1:c.303C>T	ENSP00000518501.1:p.Ser101=
ENST00000710815.1:c.303C>T	ENSP00000518502.1:p.Ser101=
ENST00000303887.10:c.624C>T MANE Select	ENSP00000307288.5:p.Ser208=
ENST00000303887.9:c.624C>T	ENSP00000307288.5:p.Ser208=
ENST00000343023.10:c.624C>T	ENSP00000344006.6:p.Ser208=
ENST00000354230.7:c.96C>T	ENSP00000346171.3:p.Ser32=
ENST00000425308.5:c.303C>T	ENSP00000411295.1:p.Ser101=
ENST00000463722.5:n.999C>T
ENST00000485286.5:n.1213C>T
ENST00000489841.5:n.775C>T
ENST00000491245.6:c.85+979C>T
ENST00000621318.4:c.96C>T	ENSP00000483795.1:p.Ser32=
NM_001278595.1:c.96C>T	NP_001265524.1:p.Ser32=
NM_005916.4:c.624C>T	NP_005907.3:p.Ser208=
NM_182776.2:c.96C>T	NP_877577.1:p.Ser32=
XM_005250348.2:c.303C>T	XP_005250405.1:p.Ser101=
XM_005250348.3:c.303C>T	XP_005250405.1:p.Ser101=
XM_017012217.2:c.303C>T	XP_016867706.1:p.Ser101=
NM_001278595.2:c.96C>T	NP_001265524.1:p.Ser32=
NM_005916.5:c.624C>T MANE Select	NP_005907.3:p.Ser208=
NM_182776.3:c.96C>T	NP_877577.1:p.Ser32=