Canonical Allele Identifier: CA2838427144

Gene: MCM4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47966421dup , CM000670.2:g.47966421dup	GRCh38
NC_000008.10:g.48878981dup , CM000670.1:g.48878981dup	GRCh37
NC_000008.9:g.49041534dup	NCBI36
NG_032967.1:g.11219dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697120.1:n.1148+14dup
ENST00000697121.1:n.1226+14dup
ENST00000697122.1:c.1053+14dup	ENSP00000513122.1:n.1053+14dup
ENST00000697123.1:n.192dup
ENST00000520637.2:c.210+146dup	ENSP00000427875.2:n.210+146dup
ENST00000647877.1:c.247-944dup
ENST00000648407.1:c.1053+14dup	ENSP00000497881.1:n.1053+14dup
ENST00000648519.1:c.*782+14dup	ENSP00000497176.1:n.*782+14dup
ENST00000649838.1:c.1053+14dup	ENSP00000497648.1:n.1053+14dup
ENST00000649919.1:c.903+14dup	ENSP00000498202.1:n.903+14dup
ENST00000649973.1:c.1053+14dup MANE Select	ENSP00000496964.1:n.1053+14dup
ENST00000650216.1:c.832+1709dup	ENSP00000497093.1:n.832+1709dup
ENST00000262105.6:c.1053+14dup	ENSP00000262105.2:n.1053+14dup
ENST00000520637.1:c.207+146dup	ENSP00000427875.1:n.207+146dup
ENST00000523944.5:c.1053+14dup	ENSP00000430194.1:n.1053+14dup
NM_005914.3:c.1053+14dup	NP_005905.2:n.1053+14dup
NM_182746.2:c.1053+14dup	NP_877423.1:n.1053+14dup
XM_005251234.1:c.903+14dup	XP_005251291.1:n.903+14dup
NM_005914.4:c.1053+14dup	NP_005905.2:n.1053+14dup
NM_182746.3:c.1053+14dup MANE Select	NP_877423.1:n.1053+14dup