Canonical Allele Identifier: CA1729340732

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098660G= , CM000669.2:g.100098660G=	GRCh38
NC_000007.13:g.99696283G= , CM000669.1:g.99696283G=	GRCh37
NC_000007.12:g.99534219G=	NCBI36
NG_016312.1:g.2154G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.317C=	ENSP00000411295.2:p.Thr106=
ENST00000485286.6:n.1250C=
ENST00000489841.6:n.1359C=
ENST00000710813.1:c.317C=	ENSP00000518500.1:p.Thr106=
ENST00000710814.1:c.317C=	ENSP00000518501.1:p.Thr106=
ENST00000710815.1:c.317C=	ENSP00000518502.1:p.Thr106=
ENST00000303887.10:c.638C= MANE Select	ENSP00000307288.5:p.Thr213=
ENST00000303887.9:c.638C=	ENSP00000307288.5:p.Thr213=
ENST00000343023.10:c.638C=	ENSP00000344006.6:p.Thr213=
ENST00000354230.7:c.110C=	ENSP00000346171.3:p.Thr37=
ENST00000425308.5:c.317C=	ENSP00000411295.1:p.Thr106=
ENST00000463722.5:n.1013C=
ENST00000485286.5:n.1227C=
ENST00000489841.5:n.789C=
ENST00000491245.6:c.85+993C=
ENST00000621318.4:c.110C=	ENSP00000483795.1:p.Thr37=
NM_001278595.1:c.110C=	NP_001265524.1:p.Thr37=
NM_005916.4:c.638C=	NP_005907.3:p.Thr213=
NM_182776.2:c.110C=	NP_877577.1:p.Thr37=
XM_005250348.2:c.317C=	XP_005250405.1:p.Thr106=
XM_005250348.3:c.317C=	XP_005250405.1:p.Thr106=
XM_017012217.2:c.317C=	XP_016867706.1:p.Thr106=
NM_001278595.2:c.110C=	NP_001265524.1:p.Thr37=
NM_005916.5:c.638C= MANE Select	NP_005907.3:p.Thr213=
NM_182776.3:c.110C=	NP_877577.1:p.Thr37=