Canonical Allele Identifier: CA368451708

Gene: MCM7

Linked Data

• MyVariant Identifiers: chr7:g.99696258A>C (hg19) ; chr7:g.100098635A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098635A>C , CM000669.2:g.100098635A>C	GRCh38
NC_000007.13:g.99696258A>C , CM000669.1:g.99696258A>C	GRCh37
NC_000007.12:g.99534194A>C	NCBI36
NG_016312.1:g.2129A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.342T>G	ENSP00000411295.2:p.Tyr114Ter
ENST00000485286.6:n.1275T>G
ENST00000489841.6:n.1384T>G
ENST00000710813.1:c.342T>G	ENSP00000518500.1:p.Tyr114Ter
ENST00000710814.1:c.342T>G	ENSP00000518501.1:p.Tyr114Ter
ENST00000710815.1:c.342T>G	ENSP00000518502.1:p.Tyr114Ter
ENST00000303887.10:c.663T>G MANE Select	ENSP00000307288.5:p.Tyr221Ter
ENST00000303887.9:c.663T>G	ENSP00000307288.5:p.Tyr221Ter
ENST00000343023.10:c.663T>G	ENSP00000344006.6:p.Tyr221Ter
ENST00000354230.7:c.135T>G	ENSP00000346171.3:p.Tyr45Ter
ENST00000425308.5:c.342T>G	ENSP00000411295.1:p.Tyr114Ter
ENST00000463722.5:n.1038T>G
ENST00000485286.5:n.1252T>G
ENST00000489841.5:n.814T>G
ENST00000491245.6:c.85+1018T>G
ENST00000621318.4:c.135T>G	ENSP00000483795.1:p.Tyr45Ter
NM_001278595.1:c.135T>G	NP_001265524.1:p.Tyr45Ter
NM_005916.4:c.663T>G	NP_005907.3:p.Tyr221Ter
NM_182776.2:c.135T>G	NP_877577.1:p.Tyr45Ter
XM_005250348.2:c.342T>G	XP_005250405.1:p.Tyr114Ter
XM_005250348.3:c.342T>G	XP_005250405.1:p.Tyr114Ter
XM_017012217.2:c.342T>G	XP_016867706.1:p.Tyr114Ter
NM_001278595.2:c.135T>G	NP_001265524.1:p.Tyr45Ter
NM_005916.5:c.663T>G MANE Select	NP_005907.3:p.Tyr221Ter
NM_182776.3:c.135T>G	NP_877577.1:p.Tyr45Ter